Glyburide
- Product NDC
- 70518-0019
- 11-digit product format
- 705180019
- Labeler code
- 70518
- Product ID
- 70518-0019_8151cd3b-0bf7-f5af-e053-2991aa0a9886
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074388
- Marketing category
- ANDA
- Marketing start
- 2016-11-28
- 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