Package 67877-843-01

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 67877-843-01
Digits Only 6787784301
Product NDC 67877-843
Description

100 TABLET, FILM COATED in 1 BOTTLE (67877-843-01)

Marketing

Marketing Status
Marketed Since 2022-07-08
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": "ea50552f-f9b9-467f-a925-62ff027df607", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0367877843056", "0367877843018", "0367877842103", "0367877842011"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245"], "spl_set_id": ["ea50552f-f9b9-467f-a925-62ff027df607"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (67877-843-01)", "package_ndc": "67877-843-01", "marketing_start_date": "20220708"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (67877-843-05)", "package_ndc": "67877-843-05", "marketing_start_date": "20220708"}], "brand_name": "FAMOTIDINE", "product_id": "67877-843_ea50552f-f9b9-467f-a925-62ff027df607", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "67877-843", "generic_name": "FAMOTIDINE", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FAMOTIDINE", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/1"}], "application_number": "ANDA215630", "marketing_category": "ANDA", "marketing_start_date": "20220708", "listing_expiration_date": "20261231"}