Glipizide
- Product NDC
- 55700-585
- 11-digit product format
- 557000585
- Labeler code
- 55700
- Product ID
- 55700-585_cebf9370-de04-4960-8290-6e49b5d6b726
- 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
- 2002-09-25
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- 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 |
|---|
| 55700-585-30 | 55700058530 | 30 TABLET in 1 BOTTLE (55700-585-30) | 30 tablet | 2018-02-16 | 0000-00-00 | No | No | Current |
| 55700-585-90 | 55700058590 | 90 TABLET in 1 BOTTLE (55700-585-90) | 90 tablet | 2018-11-16 | 0000-00-00 | No | No | Current |