Glipizide and Metformin Hydrochloride
- Product NDC
- 70518-0908
- 11-digit product format
- 705180908
- Labeler code
- 70518
- Product ID
- 70518-0908_e29a76d1-62b7-0e79-e053-2995a90a44fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078905
- Marketing category
- ANDA
- Marketing start
- 2017-12-13
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE; 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0908 | GLIPIZIDE AND METFORMIN HYDROCHLORIDE TABLET, FILM COATED [REMEDYREPACK INC.] | 17 | Legacy NDC | 20250504_b7a27f1e-6290-4649-8a93-2a48ba105618.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0908-0 | 70518090800 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0908-0) | 2017-12-13 | 0000-00-00 | No | No | Current |
| 70518-0908-1 | 70518090801 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0908-1) | 2017-12-27 | 0000-00-00 | No | No | Current |