Glyburide
- Product NDC
- 68788-7970
- 11-digit product format
- 687887970
- Labeler code
- 68788
- Product ID
- 68788-7970_5b6260ae-4f38-465f-944b-66f09c7b683d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA206483
- Marketing category
- ANDA
- Marketing start
- 2021-07-28
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68788-7970-1 | 68788797001 | 100 TABLET in 1 BOTTLE (68788-7970-1) | 100 tablet | 2021-07-28 | 0000-00-00 | No | No | Current |
| 68788-7970-3 | 68788797003 | 100 TABLET in 1 BOTTLE (68788-7970-3) | 100 tablet | 2021-07-28 | 0000-00-00 | No | No | Current |
| 68788-7970-6 | 68788797006 | 60 TABLET in 1 BOTTLE (68788-7970-6) | 60 tablet | 2021-07-28 | 0000-00-00 | No | No | Current |
| 68788-7970-9 | 68788797009 | 90 TABLET in 1 BOTTLE (68788-7970-9) | 90 tablet | 2021-07-28 | 0000-00-00 | No | No | Current |