Glyburide
- Product NDC
- 68788-6885
- 11-digit product format
- 687886885
- Labeler code
- 68788
- Product ID
- 68788-6885_25fa971d-c4ff-4ca4-89c3-0966ec0e80e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA074388
- Marketing category
- ANDA
- Marketing start
- 2017-01-30
- 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
- 2021-12-31
- 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 |
|---|
| 68788-6885-1 | 68788688501 | 100 TABLET in 1 BOTTLE (68788-6885-1) | 100 tablet | 2017-01-30 | 0000-00-00 | No | No | Current |
| 68788-6885-3 | 68788688503 | 30 TABLET in 1 BOTTLE (68788-6885-3) | 30 tablet | 2017-01-30 | 0000-00-00 | No | No | Current |
| 68788-6885-6 | 68788688506 | 60 TABLET in 1 BOTTLE (68788-6885-6) | 60 tablet | 2017-01-30 | 0000-00-00 | No | No | Current |
| 68788-6885-9 | 68788688509 | 90 TABLET in 1 BOTTLE (68788-6885-9) | 90 tablet | 2017-01-30 | 0000-00-00 | No | No | Current |