Package 31722-018-05

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 31722-018-05
Digits Only 3172201805
Product NDC 31722-018
Description

500 TABLET, FILM COATED in 1 BOTTLE (31722-018-05)

Marketing

Marketing Status
Marketed Since 2021-11-04
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": "d1215804-20c7-e3f3-e053-2a95a90aa13b", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0331722017015", "0331722018012"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["902b5d4b-1707-4312-9f46-ef5ab86b00f0"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (31722-018-01)", "package_ndc": "31722-018-01", "marketing_start_date": "20211104"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-018-05)", "package_ndc": "31722-018-05", "marketing_start_date": "20211104"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (31722-018-10)", "package_ndc": "31722-018-10", "marketing_start_date": "20211104"}], "brand_name": "Famotidine", "product_id": "31722-018_d1215804-20c7-e3f3-e053-2a95a90aa13b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "31722-018", "generic_name": "Famotidine", "labeler_name": "Camber 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"}