Glipizide
- Product NDC
- 68788-6853
- 11-digit product format
- 687886853
- Labeler code
- 68788
- Product ID
- 68788-6853_a9130dc0-33f4-4c3d-bc93-d7c7e0ebee23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA074550
- Marketing category
- ANDA
- Marketing start
- 2016-12-13
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6853-1 | 68788685301 | 100 TABLET in 1 BOTTLE (68788-6853-1) | 100 tablet | 2016-12-13 | 0000-00-00 | No | No | Current |
| 68788-6853-3 | 68788685303 | 30 TABLET in 1 BOTTLE (68788-6853-3) | 30 tablet | 2016-12-13 | 0000-00-00 | No | No | Current |
| 68788-6853-6 | 68788685306 | 60 TABLET in 1 BOTTLE (68788-6853-6) | 60 tablet | 2016-12-13 | 0000-00-00 | No | No | Current |
| 68788-6853-9 | 68788685309 | 90 TABLET in 1 BOTTLE (68788-6853-9) | 90 tablet | 2016-12-13 | 0000-00-00 | No | No | Current |