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Product Details for ANDA 075069

ETODOLAC (ETODOLAC)
400MG
Marketing Status: Discontinued
Active Ingredient: ETODOLAC
Proprietary Name: ETODOLAC
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A075069
Product Number: 001
Approval Date: Apr 16, 1998
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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