Glyburide
- Product NDC
- 42291-316
- 11-digit product format
- 422910316
- Labeler code
- 42291
- Product ID
- 42291-316_d57a9963-282f-2456-e053-2a95a90a8cd6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA074388
- Marketing category
- ANDA
- Marketing start
- 2014-09-25
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-316-50 | 42291031650 | 500 TABLET in 1 BOTTLE (42291-316-50) | 500 tablet | 2014-09-25 | 0000-00-00 | No | No | Current |