Glyburide
- Product NDC
- 49999-113
- 11-digit product format
- 499990113
- Labeler code
- 49999
- Product ID
- 49999-113_04c549eb-07cb-416f-a0d9-9efd2c7eb012
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA074388
- Marketing category
- ANDA
- Marketing start
- 2011-02-23
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE
- Active strength
- 5 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| SX6K58TVWC | GLYBURIDE | 10238-21-8 | GLYBURIDE |