Glimepiride
- Product NDC
- 0615-7523
- 11-digit product format
- 006157523
- Labeler code
- 0615
- Product ID
- 0615-7523_9b447065-35ee-4312-9f1e-ac4b4739254b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#