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LABELS · 15eaa42c-d1e7-5c08-e063-6394a90ae469

Cortrosyn

Open original source → · Download preserved record

Preserved label snapshot, not confirmation of a current approved indication. Approval/withdrawal status must be checked for the exact disease, setting and regimen.

Label effective date
2024-04-12
Captured
2026-09-09T23:37:39.774134+00:00
Current indication reconciliation
Not reconciled

Indications and usage: exact source text

  1. INDICATIONS AND USAGE CORTROSYN ® (cosyntropin) for Injection is intended for use as a diagnostic agent in the screening of patients presumed to have adrenocortical insufficiency. Because of its rapid effect on the adrenal cortex it may be utilized to perform a 30-minute test of adrenal function (plasma cortisol response) as an office or outpatient procedure, using only 2 venipunctures (see DOSAGE AND ADMINISTRATION section). Severe hypofunction of the pituitary - adrenal axis is usually associated with subnormal plasma cortisol values but a low basal level is not per se evidence of adrenal insufficiency and does not suffice to make the diagnosis. Many patients with proven insufficiency will have normal basal levels and will develop signs of insufficiency only when stressed. For this reason a criterion which should be used in establishing the diagnosis is the failure to respond to adequate corticotropin stimulation. When presumptive adrenal insufficiency is diagnosed by a subnormal CORTROSYN ® test, further studies are indicated to determine if it is primary or secondary. Primary adrenal insufficiency (Addison’s disease) is the result of an intrinsic disease process, such as tuberculosis within the gland. The production of adrenocortical hormones is deficient despite high ACTH levels (feedback mechanism). Secondary or relative insufficiency arises as the result of defective production of ACTH leading in turn to disuse atrophy of the adrenal cortex. It is commonly seen, for example, as result of corticosteroid therapy, Sheehan’s syndrome and pituitary tumors or ablation. The differentiation of both types is based on the premise that a primarily defective gland cannot be stimulated by ACTH whereas a secondarily defective gland is potentially functional and will respond to adequate stimulation with ACTH. Patients selected for further study as the result of a subnormal CORTROSYN ® test should be given a 3 or 4 day course of treatment with Repository Corticotropin Injection USP and then retested. Suggested doses are 40 USP units twice daily for 4 days or 60 USP units twice daily for 3 days. Under these conditions little or no increase in plasma cortisol levels will be seen in Addison’s disease whereas higher or even normal levels will be seen in cases with secondary adrenal insufficiency.
Full extracted label fields
application numbers
  1. NDA016750
boxed warning exact
    brand names
    1. Cortrosyn
    current indication status
    not_reconciled
    dailymed set url
    https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=15eaaab2-d656-7310-e063-6394a90ae59f
    generic names
    1. COSYNTROPIN
    id
    15eaa42c-d1e7-5c08-e063-6394a90ae469
    indications and usage exact
    1. INDICATIONS AND USAGE CORTROSYN ® (cosyntropin) for Injection is intended for use as a diagnostic agent in the screening of patients presumed to have adrenocortical insufficiency. Because of its rapid effect on the adrenal cortex it may be utilized to perform a 30-minute test of adrenal function (plasma cortisol response) as an office or outpatient procedure, using only 2 venipunctures (see DOSAGE AND ADMINISTRATION section). Severe hypofunction of the pituitary - adrenal axis is usually associated with subnormal plasma cortisol values but a low basal level is not per se evidence of adrenal insufficiency and does not suffice to make the diagnosis. Many patients with proven insufficiency will have normal basal levels and will develop signs of insufficiency only when stressed. For this reason a criterion which should be used in establishing the diagnosis is the failure to respond to adequate corticotropin stimulation. When presumptive adrenal insufficiency is diagnosed by a subnormal CORTROSYN ® test, further studies are indicated to determine if it is primary or secondary. Primary adrenal insufficiency (Addison’s disease) is the result of an intrinsic disease process, such as tuberculosis within the gland. The production of adrenocortical hormones is deficient despite high ACTH levels (feedback mechanism). Secondary or relative insufficiency arises as the result of defective production of ACTH leading in turn to disuse atrophy of the adrenal cortex. It is commonly seen, for example, as result of corticosteroid therapy, Sheehan’s syndrome and pituitary tumors or ablation. The differentiation of both types is based on the premise that a primarily defective gland cannot be stimulated by ACTH whereas a secondarily defective gland is potentially functional and will respond to adequate stimulation with ACTH. Patients selected for further study as the result of a subnormal CORTROSYN ® test should be given a 3 or 4 day course of treatment with Repository Corticotropin Injection USP and then retested. Suggested doses are 40 USP units twice daily for 4 days or 60 USP units twice daily for 3 days. Under these conditions little or no increase in plasma cortisol levels will be seen in Addison’s disease whereas higher or even normal levels will be seen in cases with secondary adrenal insufficiency.
    indications and usage tables exact
      is original packager
        manufacturer names
        1. Medical Purchasing Solutions, LLC
        matched search terms
        1. tumors
        package ndcs
        1. 71872-7318-1
        product ndcs
        1. 71872-7318
        product types
        1. HUMAN PRESCRIPTION DRUG
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            1. application number
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              payload
              all indexed label documents
              1. Appl No
                016750
                Application Docs Date
                2021-12-16 00:00:00
                Application Docs ID
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                Application Docs Title
                0
                Application Docs Type ID
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                Submission No
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                Submission Type
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              2. Appl No
                016750
                Application Docs Date
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                Application Docs ID
                77154
                Application Docs Title
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                Application Docs Type ID
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                Submission No
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                Submission Type
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                Review Priority
                STANDARD
                Submission Class Code ID
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                Submission No
                33
                Submission Status
                AP
                Submission Status Date
                2023-12-22 00:00:00
                Submission Type
                SUPPL
                Submissions Public Notes
              2. Appl No
                016750
                Review Priority
                STANDARD
                Submission Class Code ID
                3
                Submission No
                32
                Submission Status
                AP
                Submission Status Date
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                Submission Type
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                Submissions Public Notes
              3. Appl No
                016750
                Review Priority
                STANDARD
                Submission Class Code ID
                4
                Submission No
                28
                Submission Status
                AP
                Submission Status Date
                2014-09-29 00:00:00
                Submission Type
                SUPPL
                Submissions Public Notes
              4. Appl No
                016750
                Review Priority
                STANDARD
                Submission Class Code ID
                3
                Submission No
                18
                Submission Status
                AP
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                Submission Type
                SUPPL
                Submissions Public Notes
              5. Appl No
                016750
                Review Priority
                STANDARD
                Submission Class Code ID
                4
                Submission No
                17
                Submission Status
                AP
                Submission Status Date
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                Submission Type
                SUPPL
                Submissions Public Notes
              6. Appl No
                016750
                Review Priority
                STANDARD
                Submission Class Code ID
                4
                Submission No
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                Submission Status
                AP
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                1999-03-18 00:00:00
                Submission Type
                SUPPL
                Submissions Public Notes
              7. Appl No
                016750
                Review Priority
                STANDARD
                Submission Class Code ID
                3
                Submission No
                15
                Submission Status
                AP
                Submission Status Date
                1998-01-09 00:00:00
                Submission Type
                SUPPL
                Submissions Public Notes
              8. Appl No
                016750
                Review Priority
                STANDARD
                Submission Class Code ID
                4
                Submission No
                14
                Submission Status
                AP
                Submission Status Date
                1997-01-29 00:00:00
                Submission Type
                SUPPL
                Submissions Public Notes
              9. Appl No
                016750
                Review Priority
                STANDARD
                Submission Class Code ID
                4
                Submission No
                13
                Submission Status
                AP
                Submission Status Date
                1997-04-08 00:00:00
                Submission Type
                SUPPL
                Submissions Public Notes
              10. Appl No
                016750
                Review Priority
                STANDARD
                Submission Class Code ID
                4
                Submission No
                12
                Submission Status
                AP
                Submission Status Date
                1994-02-18 00:00:00
                Submission Type
                SUPPL
                Submissions Public Notes
              11. Appl No
                016750
                Review Priority
                Submission Class Code ID
                3
                Submission No
                10
                Submission Status
                AP
                Submission Status Date
                1989-04-28 00:00:00
                Submission Type
                SUPPL
                Submissions Public Notes
              12. Appl No
                016750
                Review Priority
                STANDARD
                Submission Class Code ID
                4
                Submission No
                9
                Submission Status
                AP
                Submission Status Date
                1988-10-28 00:00:00
                Submission Type
                SUPPL
                Submissions Public Notes
              application number
              NDA016750
              approval interpretation
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              current indication status
              not_reconciled
              has approved submission record
              true
              latest approved submission date
              2023-12-22
              latest label selection rule
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                Application Docs Date
                2023-12-27 00:00:00
                Application Docs ID
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                Application Docs Title
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                Application Docs Type ID
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                Submission No
                33
                Submission Type
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              official application record
              Appl No
              016750
              Appl Public Notes
              Appl Type
              NDA
              Sponsor Name
              AMPHASTAR PHARMS INC
              openfda application present
              true
              products
              1. Active Ingredient
                COSYNTROPIN
                Appl No
                016750
                Drug Name
                CORTROSYN
                Form
                INJECTABLE;INJECTION
                Product No
                001
                Reference Drug
                1
                Reference Standard
                1
                Strength
                0.25MG/VIAL
                marketing status
                1. Prescription

            Source passages and status connections

            Passage classifications are automated and are not treatment recommendations. Connections apply only to their recorded indication scope.

            Passage 1 · unclassified context
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            INDICATIONS AND USAGE CORTROSYN ® (cosyntropin) for Injection is intended for use as a diagnostic agent in the screening of patients presumed to have adrenocortical insufficiency. Because of its rapid effect on the adrenal cortex it may be utilized to perform a 30-minute test of adrenal function (plasma cortisol response) as an office or outpatient procedure, using only 2 veni
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                  INDICATIONS AND USAGE CORTROSYN ® (cosyntropin) for Injection is intended for use as a diagnostic agent in the screening of patients presumed to have adrenocortical insufficiency.
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                  INDICATIONS AND USAGE CORTROSYN ® (cosyntropin) for Injection is intended for use as a diagnostic agent in the screening of patients presumed to have adrenocortical insufficiency. Because of its rapid effect on the adrenal cortex it may be utilized to perform a 30-minute test of adrenal function (plasma cortisol response) as an office or outpatient procedure, using only 2 venipunctures (see DOSAGE AND ADMINISTRATION section). Severe hypofunction of the pituitary - adrenal axis is usually associated with subnormal plasma cortisol values but a low basal level is not per se evidence of adrenal insufficiency and does not suff
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                        Because of its rapid effect on the adrenal cortex it may be utilized to perform a 30-minute test of adrenal function (plasma cortisol response) as an office or outpatient procedure, using only 2 venipunctures (see DOSAGE AND ADMINISTRATION section).
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                        it may be utilized to perform a 30-minute test of adrenal function (plasma cortisol response) as an office or outpatient procedure, using only 2 venipunctures (see DOSAGE AND ADMINISTRATION section). Severe hypofunction of the pituitary - adrenal axis is usually associated with subnormal plasma cortisol values but a low basal level is not per se evidence of adrenal insufficiency and does not suffice to make the diagnosis. Many patients with proven insufficiency will have normal basal levels and will develop signs of insufficiency only when stressed. For this reason a criterion which should be used in establishing the
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                              Severe hypofunction of the pituitary - adrenal axis is usually associated with subnormal plasma cortisol values but a low basal level is not per se evidence of adrenal insufficiency and does not suffice to make the diagnosis.
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                              pituitary - adrenal axis is usually associated with subnormal plasma cortisol values but a low basal level is not per se evidence of adrenal insufficiency and does not suffice to make the diagnosis. Many patients with proven insufficiency will have normal basal levels and will develop signs of insufficiency only when stressed. For this reason a criterion which should be used in establishing the diagnosis is the failure to respond to adequate corticotropin stimulation. When presumptive adrenal insufficiency is diagnosed by
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                                                                              based on the premise that a primarily defective gland cannot be stimulated by ACTH whereas a secondarily defective gland is potentially functional and will respond to adequate stimulation with ACTH. Patients selected for further study as the result of a subnormal CORTROSYN ® test should be given a 3 or 4 day course of treatment with Repository Corticotropin Injection USP and then retested. Suggested doses are 40 USP units twice daily for 4 days or 60 USP units twice daily for 3 days. Under these conditions little or no increase in plasma cortisol levels will be seen in Addison’s diseas
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                                                                                  Patients selected for further study as the result of a subnormal CORTROSYN ® test should be given a 3 or 4 day course of treatment with Repository Corticotropin Injection USP and then retested.
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                                                                                  ACTH. Patients selected for further study as the result of a subnormal CORTROSYN ® test should be given a 3 or 4 day course of treatment with Repository Corticotropin Injection USP and then retested. Suggested doses are 40 USP units twice daily for 4 days or 60 USP units twice daily for 3 days. Under these conditions little or no increase in plasma cortisol levels will be seen in Addison’s disease whereas higher or even normal levels will be seen in cases with secondary adrenal insufficienc
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                                                                                        Suggested doses are 40 USP units twice daily for 4 days or 60 USP units twice daily for 3 days.
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                                                                                        e given a 3 or 4 day course of treatment with Repository Corticotropin Injection USP and then retested. Suggested doses are 40 USP units twice daily for 4 days or 60 USP units twice daily for 3 days. Under these conditions little or no increase in plasma cortisol levels will be seen in Addison’s disease whereas higher or even normal levels will be seen in cases with secondary adrenal insufficiency.
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                                                                                              Under these conditions little or no increase in plasma cortisol levels will be seen in Addison’s disease whereas higher or even normal levels will be seen in cases with secondary adrenal insufficiency.
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                                                                                              Preserved source evidence · Not medical advice