Package 72189-585-90

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 72189-585-90
Digits Only 7218958590
Product NDC 72189-585
Product ID 72189-585_230949fd-563f-8dbf-e063-6394a90ab9b6
Description

90 TABLET in 1 BOTTLE (72189-585-90)

Marketing

Marketing Status
Marketed Since 2024-09-26
Brand glimepiride
Generic glimepiride
Sample Package No

Linked Drug Pages (1)

Glimepiride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "230949fd-563f-8dbf-e063-6394a90ab9b6", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199247"], "spl_set_id": ["230949fd-563e-8dbf-e063-6394a90ab9b6"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-585-90)", "package_ndc": "72189-585-90", "marketing_start_date": "20240926"}], "brand_name": "Glimepiride", "product_id": "72189-585_230949fd-563f-8dbf-e063-6394a90ab9b6", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72189-585", "generic_name": "Glimepiride", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "4 mg/1"}], "application_number": "ANDA202112", "marketing_category": "ANDA", "marketing_start_date": "20240926", "listing_expiration_date": "20261231"}