Glyburide
- Product NDC
- 0143-9919
- 11-digit product format
- 001439919
- Labeler code
- 0143
- Product ID
- 0143-9919_2e1f1fed-bd3b-4cc5-92cc-17b78b5871cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA075890
- Marketing category
- ANDA
- Marketing start
- 2003-08-01
- 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
- 2022-12-31
- 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 |
|---|
| 0143-9919-01 | 00143991901 | 100 TABLET in 1 BOTTLE, PLASTIC (0143-9919-01) | 100 tablet | 2003-08-01 | 0000-00-00 | No | No | Current |
| 0143-9919-05 | 00143991905 | 500 TABLET in 1 BOTTLE, PLASTIC (0143-9919-05) | 500 tablet | 2003-08-01 | 0000-00-00 | No | No | Current |
| 0143-9919-10 | 00143991910 | 1000 TABLET in 1 BOTTLE, PLASTIC (0143-9919-10) | 1000 tablet | 2003-08-01 | 0000-00-00 | No | No | Current |