Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 071891

SULINDAC (SULINDAC)
150MG
Marketing Status: Prescription
Active Ingredient: SULINDAC
Proprietary Name: SULINDAC
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A071891
Product Number: 001
Approval Date: Apr 3, 1990
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Prescription
Patent and Exclusivity Information

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