Glyburide
- Product NDC
- 68071-3097
- 11-digit product format
- 680713097
- Labeler code
- 68071
- Product ID
- 68071-3097_4a51c3e8-76fd-684f-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- NDA017532
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1984-05-01
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE
- Active strength
- 3 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