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