Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 074942

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ETODOLAC (ETODOLAC)
200MG
Marketing Status: Discontinued
Active Ingredient: ETODOLAC
Proprietary Name: ETODOLAC
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A074942
Product Number: 001
Approval Date: Sep 30, 1997
Applicant Holder Full Name: SANDOZ INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
ETODOLAC (ETODOLAC)
300MG
Marketing Status: Discontinued
Active Ingredient: ETODOLAC
Proprietary Name: ETODOLAC
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A074942
Product Number: 002
Approval Date: Sep 30, 1997
Applicant Holder Full Name: SANDOZ INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

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