Package 71335-0231-4

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 71335-0231-4
Digits Only 7133502314
Product NDC 71335-0231
Description

90 TABLET in 1 BOTTLE (71335-0231-4)

Marketing

Marketing Status
Marketed Since 2018-07-16
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": "937f9913-ef4c-4251-8669-334458e0fd92", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245"], "spl_set_id": ["db3af7cc-efc6-4934-acff-8bb2d31fe829"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0231-1)", "package_ndc": "71335-0231-1", "marketing_start_date": "20180726"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0231-2)", "package_ndc": "71335-0231-2", "marketing_start_date": "20180306"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0231-3)", "package_ndc": "71335-0231-3", "marketing_start_date": "20191111"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0231-4)", "package_ndc": "71335-0231-4", "marketing_start_date": "20180716"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-0231-5)", "package_ndc": "71335-0231-5", "marketing_start_date": "20190131"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0231-6)", "package_ndc": "71335-0231-6", "marketing_start_date": "20211227"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-0231-7)", "package_ndc": "71335-0231-7", "marketing_start_date": "20211227"}], "brand_name": "Famotidine", "product_id": "71335-0231_937f9913-ef4c-4251-8669-334458e0fd92", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "71335-0231", "generic_name": "Famotidine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/1"}], "application_number": "ANDA078916", "marketing_category": "ANDA", "marketing_start_date": "20160129", "listing_expiration_date": "20261231"}