Glipizide
- Product NDC
- 42291-429
- 11-digit product format
- 422910429
- Labeler code
- 42291
- Product ID
- 42291-429_d57cc326-d855-0598-e053-2995a90acd95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA075795
- Marketing category
- ANDA
- Marketing start
- 2019-06-25
- 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
- 2023-12-31
- 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 |
|---|
| 42291-429-10 | 42291042910 | 1000 TABLET in 1 BOTTLE (42291-429-10) | 1000 tablet | 2019-06-25 | 0000-00-00 | No | No | Current |