Package 50090-7180-0

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 50090-7180-0
Digits Only 5009071800
Product NDC 50090-7180
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7180-0)

Marketing

Marketing Status
Marketed Since 2024-05-30
Brand famotidine
Generic famotidine
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c87aa6df-b23d-4398-b904-bcf303f22eeb", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["75a334ee-48b9-47e7-8225-6e595bed8a74"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7180-0)", "package_ndc": "50090-7180-0", "marketing_start_date": "20240530"}], "brand_name": "Famotidine", "product_id": "50090-7180_c87aa6df-b23d-4398-b904-bcf303f22eeb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "50090-7180", "generic_name": "Famotidine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA215767", "marketing_category": "ANDA", "marketing_start_date": "20211104", "listing_expiration_date": "20261231"}