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Metronidazole - 50111-333-06 - (Metronidazole)

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Drug Information of Metronidazole

Product NDC: 50111-333
Proprietary Name: Metronidazole
Non Proprietary Name: Metronidazole
Active Ingredient(s): 250    mg/1 & nbsp;   Metronidazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metronidazole

Product NDC: 50111-333
Labeler Name: Pliva Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070027
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Metronidazole

Package NDC: 50111-333-06
Package Description: 250 TABLET in 1 BOTTLE (50111-333-06)

NDC Information of Metronidazole

NDC Code 50111-333-06
Proprietary Name Metronidazole
Package Description 250 TABLET in 1 BOTTLE (50111-333-06)
Product NDC 50111-333
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metronidazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Pliva Inc.
Substance Name METRONIDAZOLE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient]

Complete Information of Metronidazole


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