Glyburide and Metformin Hydrochloride
- Product NDC
- 71335-0179
- 11-digit product format
- 713350179
- Labeler code
- 71335
- Product ID
- 71335-0179_2f71afe5-b072-4ff2-a6fb-76894a8f6335
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077870
- Marketing category
- ANDA
- Marketing start
- 2007-11-14
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE; METFORMIN HYDROCHLORIDE
- Active strength
- 3 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0179-1 | 71335017901 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0179-1) | 2018-03-26 | 0000-00-00 | No | No | Current |
| 71335-0179-2 | 71335017902 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0179-2) | 2018-06-08 | 0000-00-00 | No | No | Current |
| 71335-0179-3 | 71335017903 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0179-3) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0179-4 | 71335017904 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0179-4) | 2019-01-25 | 0000-00-00 | No | No | Current |
| 71335-0179-5 | 71335017905 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0179-5) | 2021-12-27 | 0000-00-00 | No | No | Current |