Package 70710-1683-0

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 70710-1683-0
Digits Only 7071016830
Product NDC 70710-1683
Description

1000 TABLET, FILM COATED in 1 BOTTLE (70710-1683-0)

Marketing

Marketing Status
Marketed Since 2022-06-06
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": "5a3e9c70-b8f8-4866-b128-9f50272c03c0", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["b165979b-7ed0-423e-9aeb-2e061df0cd45"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (70710-1683-0)", "package_ndc": "70710-1683-0", "marketing_start_date": "20220606"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1683-1)", "package_ndc": "70710-1683-1", "marketing_start_date": "20220606"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70710-1683-3)", "package_ndc": "70710-1683-3", "marketing_start_date": "20220606"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70710-1683-4)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1683-2)", "package_ndc": "70710-1683-4", "marketing_start_date": "20220606"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70710-1683-5)", "package_ndc": "70710-1683-5", "marketing_start_date": "20220606"}], "brand_name": "Famotidine", "product_id": "70710-1683_5a3e9c70-b8f8-4866-b128-9f50272c03c0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "70710-1683", "generic_name": "Famotidine", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA216441", "marketing_category": "ANDA", "marketing_start_date": "20220606", "listing_expiration_date": "20261231"}