Glimepiride
- Product NDC
- 63629-6930
- 11-digit product format
- 636296930
- Labeler code
- 63629
- Product ID
- 63629-6930_b0229a63-b428-42e1-83dc-98b7c04d1fd0
- 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
- 1 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6930-1 | 63629693001 | 30 TABLET in 1 BOTTLE (63629-6930-1) | 30 tablet | 2016-02-23 | 0000-00-00 | No | No | Current |