Glimepiride
- Product NDC
- 50090-1987
- 11-digit product format
- 500901987
- Labeler code
- 50090
- Product ID
- 50090-1987_db1f3e91-4e62-4447-9e37-52f515e0818e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078181
- Marketing category
- ANDA
- Marketing start
- 2007-08-23
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1987 | GLIMEPIRIDE TABLET [A-S MEDICATION SOLUTIONS] | 18 | Legacy NDC | 20230623_dac7b655-d2e3-458a-9a8d-677757ba2a75.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1987-0 | 50090198700 | 30 TABLET in 1 BOTTLE (50090-1987-0) | 30 tablet | 2015-09-15 | 0000-00-00 | No | No | Current |
| 50090-1987-1 | 50090198701 | 100 TABLET in 1 BOTTLE (50090-1987-1) | 100 tablet | 2015-09-15 | 0000-00-00 | No | No | Current |
| 50090-1987-2 | 50090198702 | 60 TABLET in 1 BOTTLE (50090-1987-2) | 60 tablet | 2015-09-15 | 0000-00-00 | No | No | Current |
| 50090-1987-3 | 50090198703 | 90 TABLET in 1 BOTTLE (50090-1987-3) | 90 tablet | 2015-09-15 | 0000-00-00 | No | No | Current |
| 50090-1987-4 | 50090198704 | 180 TABLET in 1 BOTTLE (50090-1987-4) | 180 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |