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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 008317

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ACTH (CORTICOTROPIN)
25 UNITS/VIAL
Marketing Status: Discontinued
Active Ingredient: CORTICOTROPIN
Proprietary Name: ACTH
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 25 UNITS/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N008317
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKEDALE PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
ACTH (CORTICOTROPIN)
40 UNITS/VIAL
Marketing Status: Discontinued
Active Ingredient: CORTICOTROPIN
Proprietary Name: ACTH
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 40 UNITS/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N008317
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKEDALE PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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