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Metronidazole - 54868-6352-0 - (metronidazole)

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Drug Information of Metronidazole

Product NDC: 54868-6352
Proprietary Name: Metronidazole
Non Proprietary Name: metronidazole
Active Ingredient(s): 7.5    mg/g & nbsp;   metronidazole
Administration Route(s): VAGINAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Metronidazole

Product NDC: 54868-6352
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020208
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120604

Package Information of Metronidazole

Package NDC: 54868-6352-0
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (54868-6352-0) > 70 g in 1 TUBE, WITH APPLICATOR

NDC Information of Metronidazole

NDC Code 54868-6352-0
Proprietary Name Metronidazole
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (54868-6352-0) > 70 g in 1 TUBE, WITH APPLICATOR
Product NDC 54868-6352
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metronidazole
Dosage Form Name GEL
Route Name VAGINAL
Start Marketing Date 20120604
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, Inc.
Substance Name METRONIDAZOLE
Strength Number 7.5
Strength Unit mg/g
Pharmaceutical Classes Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient]

Complete Information of Metronidazole


General Information