Nivestym is a Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is Filgrastim.
Product ID | 0069-0292_3a976868-6b9c-44b2-987a-3ec9cda3e7a1 |
NDC | 0069-0292 |
Product Type | Human Prescription Drug |
Proprietary Name | Nivestym |
Generic Name | Filgrastim-aafi |
Dosage Form | Injection, Solution |
Route of Administration | SUBCUTANEOUS |
Marketing Start Date | 2018-09-24 |
Marketing Category | BLA / BLA |
Application Number | BLA761080 |
Labeler Name | Pfizer Laboratories Div Pfizer Inc |
Substance Name | FILGRASTIM |
Active Ingredient Strength | 480 ug/.8mL |
Pharm Classes | Granulocyte Colony-Stimulating Factor [CS], Granulocyte-Macrophage Colony-Stimulating Factor [CS], Increased Myeloid Cell Production [PE], Leukocyte Growth Factor [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2018-09-24 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA761080 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2018-09-24 |
Marketing Category | BLA |
Application Number | BLA761080 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2018-09-24 |
Ingredient | Strength |
---|---|
FILGRASTIM | 480 ug/.8mL |
SPL SET ID: | d23ab39c-b6ec-41cf-a529-9dd2852c9d9a |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0069-0291 | Nivestym | filgrastim-aafi |
0069-0292 | Nivestym | filgrastim-aafi |
0069-0293 | Nivestym | filgrastim-aafi |
0069-0294 | Nivestym | filgrastim-aafi |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NIVESTYM 86914849 5722625 Live/Registered |
Hospira, Inc. 2016-02-22 |