Package 80005-119-16

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 80005-119-16
Digits Only 8000511916
Product NDC 80005-119
Description

50 mL in 1 BOTTLE (80005-119-16)

Marketing

Marketing Status
Marketed Since 2023-08-10
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": "7753e6db-5fe8-4b35-8817-c50abda35144", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310274"], "spl_set_id": ["45df5fae-b28a-4b48-95ef-96e4faad883f"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Carnegie Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (80005-119-16)", "package_ndc": "80005-119-16", "marketing_start_date": "20230810"}], "brand_name": "FAMOTIDINE", "product_id": "80005-119_7753e6db-5fe8-4b35-8817-c50abda35144", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "80005-119", "generic_name": "FAMOTIDINE", "labeler_name": "Carnegie Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FAMOTIDINE", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/5mL"}], "application_number": "ANDA217137", "marketing_category": "ANDA", "marketing_start_date": "20230810", "listing_expiration_date": "20261231"}