Package 70518-4394-0
Brand: famotidine
Generic: famotidinePackage Facts
Identity
Package NDC
70518-4394-0
Digits Only
7051843940
Product NDC
70518-4394
Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4394-0)
Marketing
Marketing Status
Brand
famotidine
Generic
famotidine
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a33ff4d-7fcd-fcae-e063-6294a90ad13f", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245"], "spl_set_id": ["669fbd46-cae5-4477-884e-8eca893d2e05"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4394-0)", "package_ndc": "70518-4394-0", "marketing_start_date": "20250718"}], "brand_name": "Famotidine", "product_id": "70518-4394_3a33ff4d-7fcd-fcae-e063-6294a90ad13f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "70518-4394", "generic_name": "Famotidine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/1"}], "application_number": "ANDA217400", "marketing_category": "ANDA", "marketing_start_date": "20250718", "listing_expiration_date": "20261231"}