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Metronidazole - 55289-521-21 - (Metronidazole)

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Drug Information of Metronidazole

Product NDC: 55289-521
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: 55289-521
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070033
Marketing Category: ANDA
Start Marketing Date: 20100901

Package Information of Metronidazole

Package NDC: 55289-521-21
Package Description: 21 TABLET in 1 BOTTLE, PLASTIC (55289-521-21)

NDC Information of Metronidazole

NDC Code 55289-521-21
Proprietary Name Metronidazole
Package Description 21 TABLET in 1 BOTTLE, PLASTIC (55289-521-21)
Product NDC 55289-521
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 PD-Rx Pharmaceuticals, Inc.
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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