LABELS · 7f47b815-d08b-46fe-aee9-d2cef6e86ec0
Nplate
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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
- 2026-06-23
- Captured
- 2026-09-09T23:37:51.659493+00:00
- Current indication reconciliation
- Not reconciled
Indications and usage: exact source text
- 1 INDICATIONS AND USAGE Nplate is a thrombopoietin receptor agonist indicated for the treatment of thrombocytopenia in: Adult patients with immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. ( 1.1 ) Pediatric patients 1 year of age and older with ITP for at least 6 months who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. ( 1.1 ) Nplate is indicated to increase survival in adults and in pediatric patients (including term neonates) acutely exposed to myelosuppressive doses of radiation (Hematopoietic Syndrome of Acute Radiation Syndrome [HS-ARS]). ( 1.2 ) Limitations of Use: Nplate is not indicated for the treatment of thrombocytopenia due to myelodysplastic syndrome (MDS) or any cause of thrombocytopenia other than ITP. Nplate should be used only in patients with ITP whose degree of thrombocytopenia and clinical condition increases the risk for bleeding. Nplate should not be used in an attempt to normalize platelet counts. ( 1 ) 1.1 Patients with Immune Thrombocytopenia (ITP) Nplate is indicated for the treatment of thrombocytopenia in: Adult patients with immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. Pediatric patients 1 year of age and older with ITP for at least 6 months who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. 1.2 Patients with Hematopoietic Syndrome of Acute Radiation Syndrome Nplate is indicated to increase survival in adults and in pediatric patients (including term neonates) acutely exposed to myelosuppressive doses of radiation [see Clinical Studies (14.3) ] . Limitations of Use: Nplate is not indicated for the treatment of thrombocytopenia due to myelodysplastic syndrome (MDS) or any cause of thrombocytopenia other than ITP [see Warnings and Precautions ( 5.1 )] . Nplate should be used only in patients with ITP whose degree of thrombocytopenia and clinical condition increases the risk for bleeding. Nplate should not be used in an attempt to normalize platelet counts [see Warnings and Precautions ( 5.2 )] .
Full extracted label fields
- application numbers
- BLA125268
- boxed warning exact
- brand names
- Nplate
- current indication status
- not_reconciled
- dailymed set url
- https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c45f9a58-37c1-4f76-8e36-97d38c577037
- generic names
- ROMIPLOSTIM
- id
- 7f47b815-d08b-46fe-aee9-d2cef6e86ec0
- indications and usage exact
- 1 INDICATIONS AND USAGE Nplate is a thrombopoietin receptor agonist indicated for the treatment of thrombocytopenia in: Adult patients with immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. ( 1.1 ) Pediatric patients 1 year of age and older with ITP for at least 6 months who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. ( 1.1 ) Nplate is indicated to increase survival in adults and in pediatric patients (including term neonates) acutely exposed to myelosuppressive doses of radiation (Hematopoietic Syndrome of Acute Radiation Syndrome [HS-ARS]). ( 1.2 ) Limitations of Use: Nplate is not indicated for the treatment of thrombocytopenia due to myelodysplastic syndrome (MDS) or any cause of thrombocytopenia other than ITP. Nplate should be used only in patients with ITP whose degree of thrombocytopenia and clinical condition increases the risk for bleeding. Nplate should not be used in an attempt to normalize platelet counts. ( 1 ) 1.1 Patients with Immune Thrombocytopenia (ITP) Nplate is indicated for the treatment of thrombocytopenia in: Adult patients with immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. Pediatric patients 1 year of age and older with ITP for at least 6 months who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. 1.2 Patients with Hematopoietic Syndrome of Acute Radiation Syndrome Nplate is indicated to increase survival in adults and in pediatric patients (including term neonates) acutely exposed to myelosuppressive doses of radiation [see Clinical Studies (14.3) ] . Limitations of Use: Nplate is not indicated for the treatment of thrombocytopenia due to myelodysplastic syndrome (MDS) or any cause of thrombocytopenia other than ITP [see Warnings and Precautions ( 5.1 )] . Nplate should be used only in patients with ITP whose degree of thrombocytopenia and clinical condition increases the risk for bleeding. Nplate should not be used in an attempt to normalize platelet counts [see Warnings and Precautions ( 5.2 )] .
- indications and usage tables exact
- is original packager
- true
- manufacturer names
- Amgen, Inc
- matched search terms
- myelodysplastic
- package ndcs
- 55513-222-01
- 55513-222-21
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- 55513-223-21
- 55513-221-01
- 55513-221-21
- product ndcs
- 55513-221
- 55513-222
- 55513-223
- product types
- HUMAN PRESCRIPTION DRUG
- recent major changes exact
- Warnings and Precautions, Thrombotic/Thromboembolic Complications ( 5.2 ) 02/2025 Warnings and Precautions, Loss of Response to Nplate ( 5.3 ) 02/2025
- record type
- complete_spl_indications_section_candidate
- routes
- SUBCUTANEOUS
- rxcuis
- 1728092
- 1728095
- 1728097
- 1728099
- 2201538
- 2201540
- source batch
- file
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- meta
- disclaimer
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.
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Drugs@FDA application source records
- application number
- BLA125268
- payload
- all indexed label documents
- Appl No
- 125268
- Application Docs Date
- 2008-08-25 00:00:00
- Application Docs ID
- 18827
- Application Docs Title
- 0
- Application Docs Type ID
- 2
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- Submission No
- 1
- Submission Type
- ORIG
- Appl No
- 125268
- Application Docs Date
- 2009-09-18 00:00:00
- Application Docs ID
- 18828
- Application Docs Title
- 0
- Application Docs Type ID
- 2
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- http://www.accessdata.fda.gov/drugsatfda_docs/label/2009/125268s0026lbl.pdf
- Submission No
- 26
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- Appl No
- 125268
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- 2011-12-06 00:00:00
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- 0
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- 2
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- Submission No
- 77
- Submission Type
- SUPPL
- Appl No
- 125268
- Application Docs Date
- 2014-02-11 00:00:00
- Application Docs ID
- 18830
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- 0
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- 2
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- http://www.accessdata.fda.gov/drugsatfda_docs/label/2014/125268s141lbl.pdf
- Submission No
- 141
- Submission Type
- SUPPL
- Appl No
- 125268
- Application Docs Date
- 2016-04-20 00:00:00
- Application Docs ID
- 18831
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2016/125268s155s156lbl.pdf
- Submission No
- 155
- Submission Type
- SUPPL
- Appl No
- 125268
- Application Docs Date
- 2012-11-06 00:00:00
- Application Docs ID
- 39886
- Application Docs Title
- 0
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- 2
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- Submission No
- 106
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- SUPPL
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- 125268
- Application Docs Date
- 2013-06-04 00:00:00
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- 39887
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- 0
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- 2
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- http://www.accessdata.fda.gov/drugsatfda_docs/label/2013/125268s121lbl.pdf
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- 121
- Submission Type
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- 125268
- Application Docs Date
- 2016-04-20 00:00:00
- Application Docs ID
- 39888
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- 0
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- Submission No
- 156
- Submission Type
- SUPPL
- Appl No
- 125268
- Application Docs Date
- 2017-06-06 00:00:00
- Application Docs ID
- 48658
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- 0
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- 160
- Submission Type
- SUPPL
- Appl No
- 125268
- Application Docs Date
- 2018-12-14 00:00:00
- Application Docs ID
- 56745
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- 0
- Application Docs Type ID
- 2
- Application Docs URL
- https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/125268s163lbl.pdf
- Submission No
- 163
- Submission Type
- SUPPL
- Appl No
- 125268
- Application Docs Date
- 2019-10-18 00:00:00
- Application Docs ID
- 60582
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- 0
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- 2
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- 164
- Submission Type
- SUPPL
- Appl No
- 125268
- Application Docs Date
- 2020-11-25 00:00:00
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- 65322
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- 0
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- 169
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- SUPPL
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- STANDARD
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- 176
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- 125268
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- 21
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- 2021-01-29 00:00:00
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- 125268
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- 2020-11-23 00:00:00
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- Appl No
- 125268
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 168
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- AP
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- 2021-02-10 00:00:00
- Submission Type
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- Appl No
- 125268
- Review Priority
- PRIORITY
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- 167
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- AP
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- 2021-01-28 00:00:00
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- Appl No
- 125268
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- 2019-10-17 00:00:00
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- 125268
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- Appl No
- 125268
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- 2017-06-05 00:00:00
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- Appl No
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- 156
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- approval interpretation
- Application linkage and approved submission are not indication-level current approval verification
- current indication status
- not_reconciled
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- has approved submission record
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- latest approved submission date
- 2025-02-21
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- 125268
- Application Docs Date
- 2025-02-21 00:00:00
- Application Docs ID
- 81340
- Application Docs Title
- 0
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- 125268
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- AMGEN
- openfda application present
- true
- products
- Active Ingredient
- ROMIPLOSTIM
- Appl No
- 125268
- Drug Name
- NPLATE
- Form
- INJECTABLE; SUBCUTANEOUS
- Product No
- 001
- Reference Drug
- 2
- Reference Standard
- Strength
- 250MCG/0.5ML; 500MCG/1ML.
- marketing status
- Prescription
Source passages and status connections
Passage 1 · positive indication candidate
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- 1 INDICATIONS AND USAGE Nplate is a thrombopoietin receptor agonist indicated for the treatment of thrombocytopenia in: Adult patients with immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. ( 1.1 ) Pediatric patients 1 year of age and older with ITP for at least 6 months who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. ( 1.1 ) Nplate is indicate
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- 1 INDICATIONS AND USAGE Nplate is a thrombopoietin receptor agonist indicated for the treatment of thrombocytopenia in: Adult patients with immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy.
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Passage 2 · unclassified context
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- gonist indicated for the treatment of thrombocytopenia in: Adult patients with immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. ( 1.1 ) Pediatric patients 1 year of age and older with ITP for at least 6 months who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. ( 1.1 ) Nplate is indicated to inc
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- ndicated for the treatment of thrombocytopenia in: Adult patients with immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. ( 1.1 ) Pediatric patients 1 year of age and older with ITP for at least 6 months who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. ( 1.1 ) Nplate is indicated to increase survival in adults and in pediatric patients (including term neonates) acutely exposed to myelosuppressive doses of radiation (Hematopoietic Syndrome of Acute
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Preserved source evidence · Not medical advice
Triangle