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Metronidazole - 66993-935-70 - (metronidazole)

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Drug Information of Metronidazole

Product NDC: 66993-935
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: 66993-935
Labeler Name: Prasco Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020208
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20070331

Package Information of Metronidazole

Package NDC: 66993-935-70
Package Description: 70 g in 1 TUBE, WITH APPLICATOR (66993-935-70)

NDC Information of Metronidazole

NDC Code 66993-935-70
Proprietary Name Metronidazole
Package Description 70 g in 1 TUBE, WITH APPLICATOR (66993-935-70)
Product NDC 66993-935
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metronidazole
Dosage Form Name GEL
Route Name VAGINAL
Start Marketing Date 20070331
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Prasco Laboratories
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