| Product NDC: | 42254-010 |
| Proprietary Name: | Propylthiouracil |
| Non Proprietary Name: | Propylthiouracil |
| Active Ingredient(s): | 50 mg/1 & nbsp; Propylthiouracil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42254-010 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080154 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19710723 |
| Package NDC: | 42254-010-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (42254-010-30) |
| NDC Code | 42254-010-30 |
| Proprietary Name | Propylthiouracil |
| Package Description | 30 TABLET in 1 BOTTLE (42254-010-30) |
| Product NDC | 42254-010 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propylthiouracil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19710723 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | PROPYLTHIOURACIL |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Thyroid Hormone Synthesis Inhibitor [EPC],Thyroid Hormone Synthesis Inhibitors [MoA] |