Glyburide
- Product NDC
- 68788-9216
- 11-digit product format
- 687889216
- Labeler code
- 68788
- Product ID
- 68788-9216_b5886f34-37f8-4200-b320-194a712e6da7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090937
- Marketing category
- ANDA
- Marketing start
- 2015-08-27
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record