Package 72789-427-90
Brand: famotidine
Generic: famotidinePackage Facts
Identity
Package NDC
72789-427-90
Digits Only
7278942790
Product NDC
72789-427
Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-427-90)
Marketing
Marketing Status
Brand
famotidine
Generic
famotidine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4123bcfe-adfa-2642-e063-6294a90ab06c", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0372789427904"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245"], "spl_set_id": ["2f5ec69d-926c-47a2-be47-8fef2e0ff207"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-427-90)", "package_ndc": "72789-427-90", "marketing_start_date": "20240827"}], "brand_name": "Famotidine", "product_id": "72789-427_4123bcfe-adfa-2642-e063-6294a90ab06c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "72789-427", "generic_name": "Famotidine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/1"}], "application_number": "ANDA215767", "marketing_category": "ANDA", "marketing_start_date": "20211104", "listing_expiration_date": "20261231"}