Glipizide and Metformin Hydrochloride
- Product NDC
- 63629-7249
- 11-digit product format
- 636297249
- Labeler code
- 63629
- Product ID
- 63629-7249_d1995007-9231-4229-8058-87ebc7baeb87
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077270
- Marketing category
- ANDA
- Marketing start
- 2005-10-28
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7249-1 | 63629724901 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-7249-1) | 2017-04-17 | 0000-00-00 | No | No | Current |
| 63629-7249-2 | 63629724902 | 180 TABLET, FILM COATED in 1 BOTTLE (63629-7249-2) | 2017-04-17 | 0000-00-00 | No | No | Current |