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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 089753

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ACETAZOLAMIDE (ACETAZOLAMIDE)
125MG
Marketing Status: Discontinued
Active Ingredient: ACETAZOLAMIDE
Proprietary Name: ACETAZOLAMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 125MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A089753
Product Number: 002
Approval Date: Jun 22, 1988
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
ACETAZOLAMIDE (ACETAZOLAMIDE)
250MG
Marketing Status: Discontinued
Active Ingredient: ACETAZOLAMIDE
Proprietary Name: ACETAZOLAMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A089753
Product Number: 001
Approval Date: Jun 22, 1988
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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