Glimepiride
- Product NDC
- 57237-152
- 11-digit product format
- 572370152
- Labeler code
- 57237
- Product ID
- 57237-152_15f4e6d9-4937-45fe-826a-94753b7be19a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Citron Pharma LLC
- Application
- ANDA202759
- Marketing category
- ANDA
- Marketing start
- 2012-06-29
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record