Package 70518-4486-0
Brand: glimepiride
Generic: glimepiridePackage Facts
Identity
Package NDC
70518-4486-0
Digits Only
7051844860
Product NDC
70518-4486
Description
30 TABLET in 1 BLISTER PACK (70518-4486-0)
Marketing
Marketing Status
Brand
glimepiride
Generic
glimepiride
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ff40f62-112b-3b67-e063-6394a90abf64", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199246"], "spl_set_id": ["95c59026-a2db-4579-b58c-b0a8e12e7f84"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4486-0)", "package_ndc": "70518-4486-0", "marketing_start_date": "20250929"}], "brand_name": "Glimepiride", "product_id": "70518-4486_3ff40f62-112b-3b67-e063-6394a90abf64", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "70518-4486", "generic_name": "Glimepiride", "labeler_name": "REMEDYREPACK INC.", "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": "20250929", "listing_expiration_date": "20261231"}