Package 70518-4485-1

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 70518-4485-1
Digits Only 7051844851
Product NDC 70518-4485
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-4485-1)

Marketing

Marketing Status
Marketed Since 2025-10-03
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": "42ed41d4-9928-5342-e063-6394a90af67e", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199247"], "spl_set_id": ["c994796e-dd3d-4f40-a8f2-d317f55e34d5"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-4485-0)", "package_ndc": "70518-4485-0", "marketing_start_date": "20250928"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4485-1)", "package_ndc": "70518-4485-1", "marketing_start_date": "20251003"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4485-2)", "package_ndc": "70518-4485-2", "marketing_start_date": "20251105"}], "brand_name": "Glimepiride", "product_id": "70518-4485_42ed41d4-9928-5342-e063-6394a90af67e", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "70518-4485", "generic_name": "Glimepiride", "labeler_name": "REMEDYREPACK INC.", "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": "20250928", "listing_expiration_date": "20261231"}