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Metronidazole - 68788-9887-7 - (metronidazole)

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Drug Information of Metronidazole

Product NDC: 68788-9887
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: 68788-9887
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020208
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120214

Package Information of Metronidazole

Package NDC: 68788-9887-7
Package Description: 70 g in 1 TUBE, WITH APPLICATOR (68788-9887-7)

NDC Information of Metronidazole

NDC Code 68788-9887-7
Proprietary Name Metronidazole
Package Description 70 g in 1 TUBE, WITH APPLICATOR (68788-9887-7)
Product NDC 68788-9887
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metronidazole
Dosage Form Name GEL
Route Name VAGINAL
Start Marketing Date 20120214
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Preferred 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


General Information