Tinidazole - 40032-550-08 - (Tinidazole)

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Drug Information of Tinidazole

Product NDC: 40032-550
Proprietary Name: Tinidazole
Non Proprietary Name: Tinidazole
Active Ingredient(s): 250    mg/1 & nbsp;   Tinidazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Tinidazole

Product NDC: 40032-550
Labeler Name: Novel Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202044
Marketing Category: ANDA
Start Marketing Date: 20120430

Package Information of Tinidazole

Package NDC: 40032-550-08
Package Description: 8 TABLET in 1 BOTTLE (40032-550-08)

NDC Information of Tinidazole

NDC Code 40032-550-08
Proprietary Name Tinidazole
Package Description 8 TABLET in 1 BOTTLE (40032-550-08)
Product NDC 40032-550
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tinidazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120430
Marketing Category Name ANDA
Labeler Name Novel Laboratories, Inc.
Substance Name TINIDAZOLE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient]

Complete Information of Tinidazole


General Information