Glyburide
- Product NDC
- 63187-848
- 11-digit product format
- 631870848
- Labeler code
- 63187
- Product ID
- 63187-848_031d5759-e2a4-43f4-b944-7fd30030a13a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA074388
- Marketing category
- ANDA
- Marketing start
- 1995-08-30
- Substance
- GLYBURIDE
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 63187-848-30 | 63187084830 | 30 TABLET in 1 BOTTLE (63187-848-30) | 30 tablet | 1995-08-30 | No | No | Historical |
| 63187-848-60 | 63187084860 | 60 TABLET in 1 BOTTLE (63187-848-60) | 60 tablet | 1995-08-30 | No | No | Historical |
| 63187-848-90 | 63187084890 | 90 TABLET in 1 BOTTLE (63187-848-90) | 90 tablet | 2010-03-30 | No | No | Historical |