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Metronidazole - 0168-0275-45 - (Metronidazole)

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Drug Information of Metronidazole

Product NDC: 0168-0275
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: 0168-0275
Labeler Name: E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077018
Marketing Category: ANDA
Start Marketing Date: 20060606

Package Information of Metronidazole

Package NDC: 0168-0275-45
Package Description: 1 TUBE in 1 CARTON (0168-0275-45) > 45 g in 1 TUBE

NDC Information of Metronidazole

NDC Code 0168-0275-45
Proprietary Name Metronidazole
Package Description 1 TUBE in 1 CARTON (0168-0275-45) > 45 g in 1 TUBE
Product NDC 0168-0275
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metronidazole
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20060606
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO. A division of Fougera Pharmaceuticals 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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