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Metronidazole - 63629-1386-1 - (Metronidazole)

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Drug Information of Metronidazole

Product NDC: 63629-1386
Proprietary Name: Metronidazole
Non Proprietary Name: Metronidazole
Active Ingredient(s): 500    mg/1 & nbsp;   Metronidazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metronidazole

Product NDC: 63629-1386
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070033
Marketing Category: ANDA
Start Marketing Date: 20100901

Package Information of Metronidazole

Package NDC: 63629-1386-1
Package Description: 20 TABLET in 1 BOTTLE (63629-1386-1)

NDC Information of Metronidazole

NDC Code 63629-1386-1
Proprietary Name Metronidazole
Package Description 20 TABLET in 1 BOTTLE (63629-1386-1)
Product NDC 63629-1386
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metronidazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100901
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name METRONIDAZOLE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient]

Complete Information of Metronidazole


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