Methimazole
- Product NDC
- 70934-478
- 11-digit product format
- 709340478
- Labeler code
- 70934
- Product ID
- 70934-478_a825225d-d237-07e1-e053-2995a90a44c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methimazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA040734
- Marketing category
- ANDA
- Marketing start
- 2020-02-12
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-478-30 | 70934047830 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-478-30) | 30 tablet | 2020-02-12 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rx only | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | 2020-02-12 | HUMAN PRESCRIPTION DRUG LABEL | 1 |