Glipizide
- Product NDC
- 68071-4498
- 11-digit product format
- 680714498
- Labeler code
- 68071
- Product ID
- 68071-4498_d7750461-1211-6fb1-e053-2a95a90a12d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA204720
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68071-4498-2 | 68071449802 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4498-2) | 2018-07-17 | 0000-00-00 | No | No | Current |
| 68071-4498-3 | 68071449803 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4498-3) | 2018-07-17 | 0000-00-00 | No | No | Current |
| 68071-4498-6 | 68071449806 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4498-6) | 2018-07-17 | 0000-00-00 | No | No | Current |
| 68071-4498-8 | 68071449808 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4498-8) | 2018-07-17 | 0000-00-00 | No | No | Current |