Tindamax - 54868-6155-0 - (tinidazole)

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Drug Information of Tindamax

Product NDC: 54868-6155
Proprietary Name: Tindamax
Non Proprietary Name: tinidazole
Active Ingredient(s): 500    mg/1 & nbsp;   tinidazole
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tindamax

Product NDC: 54868-6155
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021618
Marketing Category: NDA
Start Marketing Date: 20100823

Package Information of Tindamax

Package NDC: 54868-6155-0
Package Description: 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-6155-0)

NDC Information of Tindamax

NDC Code 54868-6155-0
Proprietary Name Tindamax
Package Description 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-6155-0)
Product NDC 54868-6155
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tinidazole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100823
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name TINIDAZOLE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient]

Complete Information of Tindamax


General Information