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PROCRIT
PROCRIT - 59676-320-04 - (Erythropoietin)
Drug Information of PROCRIT
| Product NDC: | 59676-320 |
| Proprietary Name: | PROCRIT |
| Non Proprietary Name: | Erythropoietin |
| Active Ingredient(s): | 20000 [iU]/mL & nbsp; Erythropoietin |
| Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROCRIT
| Product NDC: | 59676-320 |
| Labeler Name: | Janssen Products, LP |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103234 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19890601 |
Package Information of PROCRIT
| Package NDC: | 59676-320-04 |
| Package Description: | 4 VIAL, MULTI-DOSE in 1 CARTON (59676-320-04) > 1 mL in 1 VIAL, MULTI-DOSE (59676-320-00) |
NDC Information of PROCRIT
| NDC Code | 59676-320-04 |
| Proprietary Name | PROCRIT |
| Package Description | 4 VIAL, MULTI-DOSE in 1 CARTON (59676-320-04) > 1 mL in 1 VIAL, MULTI-DOSE (59676-320-00) |
| Product NDC | 59676-320 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Erythropoietin |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19890601 |
| Marketing Category Name | BLA |
| Labeler Name | Janssen Products, LP |
| Substance Name | ERYTHROPOIETIN |
| Strength Number | 20000 |
| Strength Unit | [iU]/mL |
| Pharmaceutical Classes | Erythropoiesis-stimulating Agent [EPC],Erythropoietin [Chemical/Ingredient],Increased Erythroid Cell Production [PE] |
