Glyburide and Metformin Hydrochloride
- Product NDC
- 68071-1967
- 11-digit product format
- 680711967
- Labeler code
- 68071
- Product ID
- 68071-1967_bc05e599-72f1-d75e-e053-2995a90a1087
- 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 |
|---|
| 68071-1967-2 | 68071196702 | 120 TABLET, FILM COATED in 1 BOTTLE (68071-1967-2) | 2017-02-21 | 0000-00-00 | No | No | Current |
| 68071-1967-3 | 68071196703 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-1967-3) | 2017-02-21 | 0000-00-00 | No | No | Current |
| 68071-1967-6 | 68071196706 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-1967-6) | 2017-02-21 | 0000-00-00 | No | No | Current |
| 68071-1967-8 | 68071196708 | 180 TABLET, FILM COATED in 1 BOTTLE (68071-1967-8) | 2017-02-21 | 0000-00-00 | No | No | Current |
| 68071-1967-9 | 68071196709 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-1967-9) | 2017-02-21 | 0000-00-00 | No | No | Current |