Methimazole
- Product NDC
- 71335-2906
- 11-digit product format
- 713352906
- Labeler code
- 71335
- Product ID
- 71335-2906_beff0a7e-3008-4ca1-ae01-3c3cf1a29785
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methimazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040350
- Marketing category
- ANDA
- Marketing start
- 2022-03-14
- Substance
- METHIMAZOLE
- Active strength
- 10 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 |
|---|
| 554Z48XN5E | METHIMAZOLE | 60-56-0 | METHIMAZOLE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2906-1 | 71335290601 | 100 TABLET in 1 BOTTLE (71335-2906-1) | 100 tablet | 2025-11-06 | No | No | Historical |