Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018764

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METRONIDAZOLE (METRONIDAZOLE)
250MG
Marketing Status: Discontinued

Active Ingredient: METRONIDAZOLE
Proprietary Name: METRONIDAZOLE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018764
Product Number: 001
Approval Date: Sep 17, 1982
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

METRONIDAZOLE (METRONIDAZOLE)
500MG
Marketing Status: Discontinued

Active Ingredient: METRONIDAZOLE
Proprietary Name: METRONIDAZOLE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018764
Product Number: 002
Approval Date: Dec 20, 1982
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information