Glipizide
- Product NDC
- 70934-237
- 11-digit product format
- 709340237
- Labeler code
- 70934
- Product ID
- 70934-237_afead200-67e2-3f8a-e053-2995a90a4221
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA074223
- Marketing category
- ANDA
- Marketing start
- 2019-01-11
- 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
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 |
|---|
| 70934-237-30 | 70934023730 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-237-30) | 30 tablet | 2019-01-11 | 0000-00-00 | No | No | Current |
| 70934-237-60 | 70934023760 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-237-60) | 60 tablet | 2019-07-16 | 0000-00-00 | No | No | Current |