glyburide
- Product NDC
- 50090-3012
- 11-digit product format
- 500903012
- Labeler code
- 50090
- Product ID
- 50090-3012_1822836c-2435-40f2-bbb4-7d3993e440f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA206749
- Marketing category
- ANDA
- Marketing start
- 2016-06-02
- 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