Glimepiride
- Product NDC
- 63629-6309
- 11-digit product format
- 636296309
- Labeler code
- 63629
- Product ID
- 63629-6309_e5192f73-6a4f-4fca-9bd1-e22b114bee26
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077091
- Marketing category
- ANDA
- Marketing start
- 2005-10-06
- Marketing end
- 0000-00-00
- Substance
- GLIMEPIRIDE
- Active strength
- 2 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6309-1 | 63629630901 | 30 TABLET in 1 BOTTLE (63629-6309-1) | 30 tablet | 2015-08-31 | 0000-00-00 | No | No | Current |
| 63629-6309-2 | 63629630902 | 60 TABLET in 1 BOTTLE (63629-6309-2) | 60 tablet | 2015-08-31 | 0000-00-00 | No | No | Current |
| 63629-6309-3 | 63629630903 | 120 TABLET in 1 BOTTLE (63629-6309-3) | 120 tablet | 2016-01-11 | 0000-00-00 | No | No | Current |
| 63629-6309-4 | 63629630904 | 90 TABLET in 1 BOTTLE (63629-6309-4) | 90 tablet | 2016-03-08 | 0000-00-00 | No | No | Current |