Package 72789-345-30

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 72789-345-30
Digits Only 7278934530
Product NDC 72789-345
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-345-30)

Marketing

Marketing Status
Marketed Since 2023-08-07
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": "40bb5dd9-53d8-9558-e063-6394a90a8d7f", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0372789345307"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245"], "spl_set_id": ["a3b50576-cd40-4f7e-9506-bd0a61988424"], "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": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-345-30)", "package_ndc": "72789-345-30", "marketing_start_date": "20230807"}], "brand_name": "FAMOTIDINE", "product_id": "72789-345_40bb5dd9-53d8-9558-e063-6394a90a8d7f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "72789-345", "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": "ANDA215630", "marketing_category": "ANDA", "marketing_start_date": "20220708", "listing_expiration_date": "20261231"}