Package 82868-042-90

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 82868-042-90
Digits Only 8286804290
Product NDC 82868-042
Product ID 82868-042_46dcab92-b42f-b3f1-e063-6394a90a17c3
Description

90 TABLET in 1 BOTTLE, PLASTIC (82868-042-90)

Marketing

Marketing Status
Marketed Since 2024-01-26
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": "46dcab92-b42f-b3f1-e063-6394a90a17c3", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199246"], "spl_set_id": ["10a36c79-1b24-46b7-e063-6294a90a8dca"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (82868-042-90)", "package_ndc": "82868-042-90", "marketing_start_date": "20240126"}], "brand_name": "Glimepiride", "product_id": "82868-042_46dcab92-b42f-b3f1-e063-6394a90a17c3", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "82868-042", "generic_name": "Glimepiride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "2 mg/1"}], "application_number": "ANDA202759", "marketing_category": "ANDA", "marketing_start_date": "20240126", "listing_expiration_date": "20261231"}