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H.P. Acthar - 63004-7731-1 - (Repository Corticotropin)

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Drug Information of H.P. Acthar

Product NDC: 63004-7731
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: 63004-7731
Labeler Name: Questcor Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022432
Marketing Category: NDA
Start Marketing Date: 20101015

Package Information of H.P. Acthar

Package NDC: 63004-7731-1
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (63004-7731-1) > 5 mL in 1 VIAL, MULTI-DOSE

NDC Information of H.P. Acthar

NDC Code 63004-7731-1
Proprietary Name H.P. Acthar
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (63004-7731-1) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC 63004-7731
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Repository Corticotropin
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; SUBCUTANEOUS
Start Marketing Date 20101015
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]

Complete Information of H.P. Acthar


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