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H.P. Acthar
H.P. Acthar - 63004-8710-1 - (Repository Corticotropin)
Drug Information of H.P. Acthar
| Product NDC: | 63004-8710 |
| Proprietary Name: | H.P. Acthar |
| Non Proprietary Name: | Repository Corticotropin |
| Active Ingredient(s): | 80 [USP'U]/mL & nbsp; Repository Corticotropin |
| Administration Route(s): | INTRAMUSCULAR; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of H.P. Acthar
| Product NDC: | 63004-8710 |
| Labeler Name: | Questcor Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022432 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130107 |
Package Information of H.P. Acthar
| Package NDC: | 63004-8710-1 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (63004-8710-1) > 5 mL in 1 VIAL, MULTI-DOSE |
NDC Information of H.P. Acthar
| NDC Code | 63004-8710-1 |
| Proprietary Name | H.P. Acthar |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (63004-8710-1) > 5 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 63004-8710 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Repository Corticotropin |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; SUBCUTANEOUS |
| Start Marketing Date | 20130107 |
| Marketing Category Name | NDA |
| Labeler Name | Questcor Pharmaceuticals, Inc. |
| Substance Name | CORTICOTROPIN |
| Strength Number | 80 |
| Strength Unit | [USP'U]/mL |
| Pharmaceutical Classes | Adrenocorticotropic Hormone [Chemical/Ingredient],Adrenocorticotropic Hormone [EPC] |
