Package 70518-3504-1

Brand: glyburide

Generic: glyburide
NDC Package

Package Facts

Identity

Package NDC 70518-3504-1
Digits Only 7051835041
Product NDC 70518-3504
Description

30 TABLET in 1 BLISTER PACK (70518-3504-1)

Marketing

Marketing Status
Marketed Since 2024-02-12
Brand glyburide
Generic glyburide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3aae409d-723d-57ca-e063-6394a90ae78b", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["SX6K58TVWC"], "rxcui": ["310534"], "spl_set_id": ["e23b9a3b-0184-4d1c-8e2c-668697a6da87"], "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 (70518-3504-1)", "package_ndc": "70518-3504-1", "marketing_start_date": "20240212"}], "brand_name": "Glyburide", "product_id": "70518-3504_3aae409d-723d-57ca-e063-6394a90ae78b", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "70518-3504", "generic_name": "Glyburide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glyburide", "active_ingredients": [{"name": "GLYBURIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA203379", "marketing_category": "ANDA", "marketing_start_date": "20220831", "listing_expiration_date": "20261231"}