Glipizide
- Product NDC
- 68788-7553
- 11-digit product format
- 687887553
- Labeler code
- 68788
- Product ID
- 68788-7553_6162bf75-1ff3-4931-8bf3-550a59a84c86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA206928
- Marketing category
- ANDA
- Marketing start
- 2017-05-12
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7553-1 | 68788755301 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7553-1) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7553-3 | 68788755303 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7553-3) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7553-6 | 68788755306 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7553-6) | 2019-10-04 | 0000-00-00 | No | No | Current |
| 68788-7553-9 | 68788755309 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7553-9) | 2019-10-04 | 0000-00-00 | No | No | Current |