Glimepiride
- Product NDC
- 69543-123
- 11-digit product format
- 695430123
- Labeler code
- 69543
- Product ID
- 69543-123_d8f2bca6-5e18-4a1f-b782-9b6e7ba83bc3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Virtus Pharmaceuticals
- Application
- ANDA202112
- Marketing category
- ANDA
- Marketing start
- 2015-07-14
- Marketing end
- 0000-00-00
- Substance
- GLIMEPIRIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69543-123 | GLIMEPIRIDE TABLET [VIRTUS PHARMACEUTICALS] | 3 | Legacy NDC | 20190403_4419ca50-539c-47e8-ab00-dbb45c7c1814.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69543-123-10 | 69543012310 | 100 TABLET in 1 BOTTLE (69543-123-10) | 100 tablet | 2015-07-14 | 0000-00-00 | No | No | Current |
| 69543-123-50 | 69543012350 | 500 TABLET in 1 BOTTLE (69543-123-50) | 500 tablet | 2015-07-14 | 0000-00-00 | No | No | Current |