Package 71205-781-30

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 71205-781-30
Digits Only 7120578130
Product NDC 71205-781
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-781-30)

Marketing

Marketing Status
Marketed Since 2023-03-27
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": "fe21daca-ac48-4b46-9cb3-9a69af0c6a84", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0371205781903"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245"], "spl_set_id": ["fe21daca-ac48-4b46-9cb3-9a69af0c6a84"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-781-30)", "package_ndc": "71205-781-30", "marketing_start_date": "20230327"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-781-60)", "package_ndc": "71205-781-60", "marketing_start_date": "20230327"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-781-90)", "package_ndc": "71205-781-90", "marketing_start_date": "20230327"}], "brand_name": "Famotidine", "product_id": "71205-781_fe21daca-ac48-4b46-9cb3-9a69af0c6a84", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "71205-781", "generic_name": "Famotidine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/1"}], "application_number": "ANDA075511", "marketing_category": "ANDA", "marketing_start_date": "20010416", "listing_expiration_date": "20261231"}