PROPYLTHIOURACIL
- Product NDC
- 71335-2901
- 11-digit product format
- 713352901
- Labeler code
- 71335
- Product ID
- 71335-2901_abe2d5d5-aac6-442a-a2b7-1a6eccd2297b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROPYLTHIOURACIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA080154
- Marketing category
- ANDA
- Marketing start
- 2021-03-18
- Substance
- PROPYLTHIOURACIL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Thyroid Hormone Synthesis Inhibitor [EPC], Thyroid Hormone Synthesis Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 721M9407IY | PROPYLTHIOURACIL | 51-52-5 | PROPYLTHIOURACIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2901-1 | 71335290101 | 100 TABLET in 1 BOTTLE (71335-2901-1) | 100 tablet | 2025-11-11 | No | No | Historical |