Glyburide and Metformin Hydrochloride
- Product NDC
- 68071-4828
- 11-digit product format
- 680714828
- Labeler code
- 68071
- Product ID
- 68071-4828_bb8feade-61be-adcc-e053-2995a90aa418
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077870
- Marketing category
- ANDA
- Marketing start
- 2007-11-14
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE; METFORMIN HYDROCHLORIDE
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4828-1 | 68071482801 | 100 TABLET, FILM COATED in 1 BOTTLE (68071-4828-1) | 2019-04-02 | 0000-00-00 | No | No | Current |