Package 72205-145-05

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 72205-145-05
Digits Only 7220514505
Product NDC 72205-145
Description

500 TABLET, FILM COATED in 1 BOTTLE (72205-145-05)

Marketing

Marketing Status
Marketed Since 2024-09-18
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": "34acb853-6632-49cd-970a-e6fd840852d3", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0372205146990", "0372205145504", "0372205145054", "0372205146051", "0372205145306", "0372205145986", "0372205145917", "0372205146914", "0372205145993", "0372205146303"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["74a24590-a0b6-4607-8e67-9fadce53389b"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72205-145-05)", "package_ndc": "72205-145-05", "marketing_start_date": "20240918"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72205-145-30)", "package_ndc": "72205-145-30", "marketing_start_date": "20240918"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (72205-145-50)", "package_ndc": "72205-145-50", "marketing_start_date": "20251112"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72205-145-91)", "package_ndc": "72205-145-91", "marketing_start_date": "20240918"}, {"sample": false, "description": "75 TABLET, FILM COATED in 1 BOTTLE (72205-145-98)", "package_ndc": "72205-145-98", "marketing_start_date": "20251112"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72205-145-99)", "package_ndc": "72205-145-99", "marketing_start_date": "20240918"}], "brand_name": "Famotidine", "product_id": "72205-145_34acb853-6632-49cd-970a-e6fd840852d3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "72205-145", "generic_name": "Famotidine", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA217400", "marketing_category": "ANDA", "marketing_start_date": "20240806", "listing_expiration_date": "20261231"}