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Tinidazole
Tinidazole - 40032-550-08 - (Tinidazole)
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] |
