Glipizide
- Product NDC
- 68071-3009
- 11-digit product format
- 680713009
- Labeler code
- 68071
- Product ID
- 68071-3009_bb12a06b-0077-3cef-e053-2995a90a1ca1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA074550
- Marketing category
- ANDA
- Marketing start
- 2011-07-18
- 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
- 2022-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3009-2 | 68071300902 | 120 TABLET in 1 BOTTLE (68071-3009-2) | 120 tablet | 2017-03-09 | 0000-00-00 | No | No | Current |
| 68071-3009-3 | 68071300903 | 30 TABLET in 1 BOTTLE (68071-3009-3) | 30 tablet | 2017-03-09 | 0000-00-00 | No | No | Current |
| 68071-3009-6 | 68071300906 | 60 TABLET in 1 BOTTLE (68071-3009-6) | 60 tablet | 2017-03-09 | 0000-00-00 | No | No | Current |
| 68071-3009-8 | 68071300908 | 180 TABLET in 1 BOTTLE (68071-3009-8) | 180 tablet | 2017-03-09 | 0000-00-00 | No | No | Current |
| 68071-3009-9 | 68071300909 | 90 TABLET in 1 BOTTLE (68071-3009-9) | 90 tablet | 2017-03-09 | 0000-00-00 | No | No | Current |