Glyburide
- Product NDC
- 63629-2907
- 11-digit product format
- 636292907
- Labeler code
- 63629
- Product ID
- 63629-2907_bb805b5d-cb45-4ae1-bbc7-45c69b755fed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074388
- Marketing category
- ANDA
- Marketing start
- 1995-08-30
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| SX6K58TVWC | GLYBURIDE | 10238-21-8 | GLYBURIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2907-1 | 63629290701 | 30 TABLET in 1 BOTTLE (63629-2907-1) | 30 tablet | 2005-08-09 | 0000-00-00 | No | No | Current |
| 63629-2907-2 | 63629290702 | 60 TABLET in 1 BOTTLE (63629-2907-2) | 60 tablet | 2005-08-09 | 0000-00-00 | No | No | Current |
| 63629-2907-3 | 63629290703 | 90 TABLET in 1 BOTTLE (63629-2907-3) | 90 tablet | 2005-08-09 | 0000-00-00 | No | No | Current |