Package 67877-889-01

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 67877-889-01
Digits Only 6787788901
Product NDC 67877-889
Description

100 TABLET, FILM COATED in 1 BOTTLE (67877-889-01)

Marketing

Marketing Status
Marketed Since 2023-08-23
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": "23381364-14e1-4f63-aea4-66d605fd14f1", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0367877842011"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["be69d9f9-f4ad-4cfe-bab2-e07186b25c1e"], "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 (67877-889-01)", "package_ndc": "67877-889-01", "marketing_start_date": "20230823"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (67877-889-05)", "package_ndc": "67877-889-05", "marketing_start_date": "20230823"}], "brand_name": "FAMOTIDINE", "product_id": "67877-889_23381364-14e1-4f63-aea4-66d605fd14f1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "67877-889", "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": "20230823", "listing_expiration_date": "20261231"}