glyburide and metformin hydrochloride
- Product NDC
- 71335-0114
- 11-digit product format
- 713350114
- Labeler code
- 71335
- Product ID
- 71335-0114_0fbe486c-e21a-48e4-8768-a43cc3b76657
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glyburide and metformin hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206748
- Marketing category
- ANDA
- Marketing start
- 2016-04-07
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE; METFORMIN HYDROCHLORIDE
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS], 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 |
|---|
| 71335-0114-1 | 71335011401 | 30 TABLET in 1 BOTTLE (71335-0114-1) | 30 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0114-3 | 71335011403 | 60 TABLET in 1 BOTTLE (71335-0114-3) | 60 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0114-4 | 71335011404 | 90 TABLET in 1 BOTTLE (71335-0114-4) | 90 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0114-5 | 71335011405 | 120 TABLET in 1 BOTTLE (71335-0114-5) | 120 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0114-6 | 71335011406 | 100 TABLET in 1 BOTTLE (71335-0114-6) | 100 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0114-7 | 71335011407 | 180 TABLET in 1 BOTTLE (71335-0114-7) | 180 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0114-8 | 71335011408 | 25 TABLET in 1 BOTTLE (71335-0114-8) | 25 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |