glipizide and metformin hcl
- Product NDC
- 70518-2196
- 11-digit product format
- 705182196
- Labeler code
- 70518
- Product ID
- 70518-2196_eeb3c173-b27f-76e4-e053-2995a90a0e79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glipizide and metformin hcl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078728
- Marketing category
- ANDA
- Marketing start
- 2019-07-09
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE; 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 |
|---|
| 70518-2196-0 | 70518219600 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2196-0) | 2019-07-09 | 0000-00-00 | No | No | Current |