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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 215737

CETRORELIX ACETATE (CETRORELIX ACETATE)
EQ 0.25MG BASE/VIAL
Marketing Status: Prescription
Active Ingredient: CETRORELIX ACETATE
Proprietary Name: CETRORELIX ACETATE
Dosage Form; Route of Administration: POWDER; SUBCUTANEOUS
Strength: EQ 0.25MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A215737
Product Number: 001
Approval Date: Aug 12, 2022
Applicant Holder Full Name: AKORN OPERATING CO LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
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