Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018241

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ALLOPURINOL (ALLOPURINOL)
100MG
Marketing Status: Discontinued

Active Ingredient: ALLOPURINOL
Proprietary Name: ALLOPURINOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018241
Product Number: 001
Approval Date: Nov 16, 1984
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

ALLOPURINOL (ALLOPURINOL)
300MG
Marketing Status: Discontinued

Active Ingredient: ALLOPURINOL
Proprietary Name: ALLOPURINOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018241
Product Number: 002
Approval Date: Nov 16, 1984
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information