Methimazole
- Product NDC
- 50436-7066
- 11-digit product format
- 504367066
- Labeler code
- 50436
- Product ID
- 50436-7066_38fbfe5d-149f-4310-b16b-a56968eacc77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methimazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA040411
- Marketing category
- ANDA
- Marketing start
- 2001-03-27
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record