Glipizide
- Product NDC
- 50090-0503
- 11-digit product format
- 500900503
- Labeler code
- 50090
- Product ID
- 50090-0503_4401f1cb-4b83-471b-94e4-ae01f90a93be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074223
- Marketing category
- ANDA
- Marketing start
- 1995-02-27
- 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 |
|---|
| 50090-0503-0 | 50090050300 | 30 TABLET in 1 BOTTLE (50090-0503-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0503-1 | 50090050301 | 60 TABLET in 1 BOTTLE (50090-0503-1) | 60 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0503-2 | 50090050302 | 100 TABLET in 1 BOTTLE (50090-0503-2) | 100 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0503-4 | 50090050304 | 200 TABLET in 1 BOTTLE (50090-0503-4) | 200 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0503-5 | 50090050305 | 90 TABLET in 1 BOTTLE (50090-0503-5) | 90 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0503-6 | 50090050306 | 180 TABLET in 1 BOTTLE (50090-0503-6) | 180 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |