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FDA Drug Approval, N019737, METROGEL
FDA Drug Approval, N019737, METROGEL
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NDA: 019737
Company: GALDERMA LABS LP
Drug Name: METROGEL
Active Ingredients: METRONIDAZOLE
Strength: 0.75%
Dosage Form/Route: GEL;TOPICAL
Action Date: 11/22/1988
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
Company: GALDERMA LABS LP
Drug Name: METROGEL
Active Ingredients: METRONIDAZOLE
Strength: 0.75%
Dosage Form/Route: GEL;TOPICAL
Action Date: 11/22/1988
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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