Glyburide
- Product NDC
- 70934-715
- 11-digit product format
- 709340715
- Labeler code
- 70934
- Product ID
- 70934-715_a9ddaacf-94e2-31a2-e053-2995a90a8687
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA074388
- Marketing category
- ANDA
- Marketing start
- 2020-05-19
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE
- Active strength
- 5 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 |
|---|
| 70934-715-90 | 70934071590 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-715-90) | 90 tablet | 2020-05-19 | 0000-00-00 | No | No | Current |