Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018894

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TOLAZAMIDE (TOLAZAMIDE)
100MG
Marketing Status: Discontinued

Active Ingredient: TOLAZAMIDE
Proprietary Name: TOLAZAMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018894
Product Number: 001
Approval Date: Nov 2, 1984
Applicant Holder Full Name: COSETTE PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

TOLAZAMIDE (TOLAZAMIDE)
250MG
Marketing Status: Discontinued

Active Ingredient: TOLAZAMIDE
Proprietary Name: TOLAZAMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018894
Product Number: 002
Approval Date: Nov 2, 1984
Applicant Holder Full Name: COSETTE PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

TOLAZAMIDE (TOLAZAMIDE)
500MG
Marketing Status: Discontinued

Active Ingredient: TOLAZAMIDE
Proprietary Name: TOLAZAMIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018894
Product Number: 003
Approval Date: Nov 2, 1984
Applicant Holder Full Name: COSETTE PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information