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Metronidazole - 49349-034-02 - (Metronidazole)

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Drug Information of Metronidazole

Product NDC: 49349-034
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: 49349-034
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070035
Marketing Category: ANDA
Start Marketing Date: 20101010

Package Information of Metronidazole

Package NDC: 49349-034-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-034-02)

NDC Information of Metronidazole

NDC Code 49349-034-02
Proprietary Name Metronidazole
Package Description 30 TABLET in 1 BLISTER PACK (49349-034-02)
Product NDC 49349-034
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metronidazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101010
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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