Glipizide
- Product NDC
- 71335-1592
- 11-digit product format
- 713351592
- Labeler code
- 71335
- Product ID
- 71335-1592_db64d70d-5602-4431-abde-5cf8e8d92afe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206928
- Marketing category
- ANDA
- Marketing start
- 2017-05-12
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 5 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| X7WDT95N5C | GLIPIZIDE | 29094-61-9 | GLIPIZIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1592-1 | 71335159201 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1592-1) | 2020-05-08 | 0000-00-00 | No | No | Current |
| 71335-1592-2 | 71335159202 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1592-2) | 2020-05-08 | 0000-00-00 | No | No | Current |
| 71335-1592-3 | 71335159203 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1592-3) | 2020-05-08 | 0000-00-00 | No | No | Current |
| 71335-1592-4 | 71335159204 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1592-4) | 2020-05-08 | 0000-00-00 | No | No | Current |