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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 071362

MECLOFENAMATE SODIUM (MECLOFENAMATE SODIUM)
EQ 50MG BASE
Marketing Status: Discontinued
Active Ingredient: MECLOFENAMATE SODIUM
Proprietary Name: MECLOFENAMATE SODIUM
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 50MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A071362
Product Number: 001
Approval Date: Feb 10, 1987
Applicant Holder Full Name: AMERICAN THERAPEUTICS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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