Package 72189-453-90

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 72189-453-90
Digits Only 7218945390
Product NDC 72189-453
Product ID 72189-453_2c4dbbad-3ed6-fec3-e063-6394a90a3b4d
Description

90 TABLET in 1 BOTTLE (72189-453-90)

Marketing

Marketing Status
Marketed Since 2023-03-24
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": "2c4dbbad-3ed6-fec3-e063-6394a90a3b4d", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199247"], "spl_set_id": ["f7a9cca6-e460-c9d2-e053-6294a90af51b"], "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 (72189-453-90)", "package_ndc": "72189-453-90", "marketing_start_date": "20230324"}], "brand_name": "Glimepiride", "product_id": "72189-453_2c4dbbad-3ed6-fec3-e063-6394a90a3b4d", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72189-453", "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": "20230324", "listing_expiration_date": "20261231"}