Glimepiride
- Product NDC
- 50090-2485
- 11-digit product format
- 500902485
- Labeler code
- 50090
- Product ID
- 50090-2485_849fb560-7b22-4277-bd53-b508ef6f859e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077911
- Marketing category
- ANDA
- Marketing start
- 2012-01-01
- 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
- 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 |
|---|
| 50090-2485-2 | 50090248502 | 60 TABLET in 1 BOTTLE, PLASTIC (50090-2485-2) | 60 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-2485-4 | 50090248504 | 180 TABLET in 1 BOTTLE, PLASTIC (50090-2485-4) | 180 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |