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Metronidazole - 49349-164-02 - (Metronidazole)

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Drug Information of Metronidazole

Product NDC: 49349-164
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: 49349-164
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070044
Marketing Category: ANDA
Start Marketing Date: 20110413

Package Information of Metronidazole

Package NDC: 49349-164-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-164-02)

NDC Information of Metronidazole

NDC Code 49349-164-02
Proprietary Name Metronidazole
Package Description 30 TABLET in 1 BLISTER PACK (49349-164-02)
Product NDC 49349-164
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metronidazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110413
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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