Package 67046-1608-3

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 67046-1608-3
Digits Only 6704616083
Product NDC 67046-1608
Description

30 TABLET in 1 BLISTER PACK (67046-1608-3)

Marketing

Marketing Status
Marketed Since 2025-10-22
Brand glimepiride
Generic glimepiride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c0ccac-2fbc-0fe2-e063-6294a90a2a9c", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199246"], "spl_set_id": ["41bf4a72-9288-50a1-e063-6394a90a5e7c"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1608-3)", "package_ndc": "67046-1608-3", "marketing_start_date": "20251022"}], "brand_name": "Glimepiride", "product_id": "67046-1608_48c0ccac-2fbc-0fe2-e063-6294a90a2a9c", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "67046-1608", "generic_name": "Glimepiride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "2 mg/1"}], "application_number": "ANDA202112", "marketing_category": "ANDA", "marketing_start_date": "20251022", "listing_expiration_date": "20271231"}