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Thiola
Thiola - 0178-0900-01 - (tiopronin)
Drug Information of Thiola
| Product NDC: | 0178-0900 |
| Proprietary Name: | Thiola |
| Non Proprietary Name: | tiopronin |
| Active Ingredient(s): | 100 mg/1 & nbsp; tiopronin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, SUGAR COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Thiola
| Product NDC: | 0178-0900 |
| Labeler Name: | Mission Pharmacal Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019569 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19880811 |
Package Information of Thiola
| Package NDC: | 0178-0900-01 |
| Package Description: | 100 TABLET, SUGAR COATED in 1 BOTTLE (0178-0900-01) |
NDC Information of Thiola
| NDC Code | 0178-0900-01 |
| Proprietary Name | Thiola |
| Package Description | 100 TABLET, SUGAR COATED in 1 BOTTLE (0178-0900-01) |
| Product NDC | 0178-0900 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tiopronin |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 19880811 |
| Marketing Category Name | NDA |
| Labeler Name | Mission Pharmacal Company |
| Substance Name | TIOPRONIN |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cystine Disulfide Reduction [MoA],N-substituted Glycines [Chemical/Ingredient],Reducing and Complexing Thiol [EPC] |
