Glyburide
- Product NDC
- 66267-102
- 11-digit product format
- 662670102
- Labeler code
- 66267
- Product ID
- 66267-102_b8a71017-8702-1b3f-e053-2995a90a2414
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA090937
- Marketing category
- ANDA
- Marketing start
- 2010-10-05
- 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 |
|---|
| 66267-102-30 | 66267010230 | 30 TABLET in 1 BOTTLE (66267-102-30) | 30 tablet | 2016-10-06 | 0000-00-00 | No | No | Current |
| 66267-102-60 | 66267010260 | 60 TABLET in 1 BOTTLE (66267-102-60) | 60 tablet | 2016-10-06 | 0000-00-00 | No | No | Current |
| 66267-102-90 | 66267010290 | 90 TABLET in 1 BOTTLE (66267-102-90) | 90 tablet | 2016-10-06 | 0000-00-00 | No | No | Current |