Glipizide
- Product NDC
- 66267-100
- 11-digit product format
- 662670100
- Labeler code
- 66267
- Product ID
- 66267-100_9cbd3056-3c1c-916d-e053-2a95a90aa243
- 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
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66267-100-30 | 66267010030 | 30 TABLET in 1 BOTTLE (66267-100-30) | 30 tablet | 2016-10-06 | 0000-00-00 | No | No | Current |
| 66267-100-60 | 66267010060 | 60 TABLET in 1 BOTTLE (66267-100-60) | 60 tablet | 2016-10-06 | 0000-00-00 | No | No | Current |
| 66267-100-90 | 66267010090 | 90 TABLET in 1 BOTTLE (66267-100-90) | 90 tablet | 2016-10-06 | 0000-00-00 | No | No | Current |
| 66267-100-91 | 66267010091 | 120 TABLET in 1 BOTTLE (66267-100-91) | 120 tablet | 2016-10-06 | 0000-00-00 | No | No | Current |
| 66267-100-92 | 66267010092 | 180 TABLET in 1 BOTTLE (66267-100-92) | 180 tablet | 2016-10-06 | 0000-00-00 | No | No | Current |