Glipizide and Metformin Hydrochloride
- Product NDC
- 71335-1778
- 11-digit product format
- 713351778
- Labeler code
- 71335
- Product ID
- 71335-1778_a9b480a1-42e4-424b-9563-27c01f06b7c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078905
- Marketing category
- ANDA
- Marketing start
- 2016-05-05
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE; 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1778-1 | 71335177801 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1778-1) | 2021-03-11 | 0000-00-00 | No | No | Current |
| 71335-1778-2 | 71335177802 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1778-2) | 2021-03-11 | 0000-00-00 | No | No | Current |
| 71335-1778-3 | 71335177803 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1778-3) | 2021-03-11 | 0000-00-00 | No | No | Current |