GLIMEPIRIDE
- Product NDC
- 60760-230
- 11-digit product format
- 607600230
- Labeler code
- 60760
- Product ID
- 60760-230_a23cdd03-157a-0a4f-e053-2995a90a10ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLIMEPIRIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St Marys Medical Park Pharmacy
- Application
- ANDA077091
- Marketing category
- ANDA
- Marketing start
- 2013-05-09
- Marketing end
- 0000-00-00
- Substance
- GLIMEPIRIDE
- Active strength
- 4 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-230-90 | 60760023090 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-230-90) | 90 tablet | 2020-03-31 | 0000-00-00 | No | No | Current |