Package 80425-0329-2
Brand: famotidine
Generic: famotidinePackage Facts
Identity
Package NDC
80425-0329-2
Digits Only
8042503292
Product NDC
80425-0329
Description
60 TABLET, FILM COATED in 1 BOTTLE (80425-0329-2)
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": "2a9c0c91-2b34-4def-e063-6294a90a58ef", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["fa18ed52-f038-02dd-e053-6394a90ac946"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0329-1)", "package_ndc": "80425-0329-1", "marketing_start_date": "20230424"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0329-2)", "package_ndc": "80425-0329-2", "marketing_start_date": "20230424"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0329-3)", "package_ndc": "80425-0329-3", "marketing_start_date": "20230424"}], "brand_name": "Famotidine", "product_id": "80425-0329_2a9c0c91-2b34-4def-e063-6294a90a58ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "80425-0329", "generic_name": "Famotidine", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA215767", "marketing_category": "ANDA", "marketing_start_date": "20230424", "listing_expiration_date": "20261231"}