Glimepiride
- Product NDC
- 68788-6801
- 11-digit product format
- 687886801
- Labeler code
- 68788
- Product ID
- 68788-6801_086422df-9b39-4a94-9e46-4bf43c1609b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA091220
- Marketing category
- ANDA
- Marketing start
- 2016-11-03
- Marketing end
- 0000-00-00
- Substance
- GLIMEPIRIDE
- Active strength
- 2 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