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Metronidazole - 0115-1474-46 - (Metronidazole)

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Drug Information of Metronidazole

Product NDC: 0115-1474
Proprietary Name: Metronidazole
Non Proprietary Name: Metronidazole
Active Ingredient(s): 7.5    mg/g & nbsp;   Metronidazole
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Metronidazole

Product NDC: 0115-1474
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077547
Marketing Category: ANDA
Start Marketing Date: 20060713

Package Information of Metronidazole

Package NDC: 0115-1474-46
Package Description: 1 TUBE in 1 CARTON (0115-1474-46) > 45 g in 1 TUBE

NDC Information of Metronidazole

NDC Code 0115-1474-46
Proprietary Name Metronidazole
Package Description 1 TUBE in 1 CARTON (0115-1474-46) > 45 g in 1 TUBE
Product NDC 0115-1474
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metronidazole
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20060713
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories Inc.
Substance Name METRONIDAZOLE
Strength Number 7.5
Strength Unit mg/g
Pharmaceutical Classes Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient]

Complete Information of Metronidazole


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