Glipizide
- Product NDC
- 55700-624
- 11-digit product format
- 557000624
- Labeler code
- 55700
- Product ID
- 55700-624_b7ed2b36-bcd3-403b-b6ae-e8b511b41729
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA075795
- Marketing category
- ANDA
- Marketing start
- 2018-05-18
- 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
- 2020-12-31
- 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 |
|---|
| 55700-624-30 | 55700062430 | 30 TABLET in 1 BOTTLE (55700-624-30) | 30 tablet | 2018-05-18 | 0000-00-00 | No | No | Current |
| 55700-624-60 | 55700062460 | 60 TABLET in 1 BOTTLE (55700-624-60) | 60 tablet | 2018-10-19 | 0000-00-00 | No | No | Current |
| 55700-624-90 | 55700062490 | 90 TABLET in 1 BOTTLE (55700-624-90) | 90 tablet | 2018-05-18 | 0000-00-00 | No | No | Current |