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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 075274

NALTREXONE HYDROCHLORIDE (NALTREXONE HYDROCHLORIDE)
50MG
Marketing Status: Prescription
Active Ingredient: NALTREXONE HYDROCHLORIDE
Proprietary Name: NALTREXONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075274
Product Number: 001
Approval Date: May 26, 1999
Applicant Holder Full Name: ELITE LABORATORIES INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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