Package 54257-802-02
Brand: famotidine
Generic: famotidinePackage Facts
Identity
Package NDC
54257-802-02
Digits Only
5425780202
Product NDC
54257-802
Description
100 TABLET, FILM COATED in 1 BOTTLE (54257-802-02)
Marketing
Marketing Status
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": "54c5dd3f-7261-47e2-adfc-23ef9955eb39", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0043292564720"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["f5d5b40e-82e5-4284-9f3f-d2c0e88f0ab9"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Magno-Humphries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (54257-802-02)", "package_ndc": "54257-802-02", "marketing_start_date": "20160426"}], "brand_name": "Famotidine", "product_id": "54257-802_54c5dd3f-7261-47e2-adfc-23ef9955eb39", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "54257-802", "generic_name": "Famotidine", "labeler_name": "Magno-Humphries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA206531", "marketing_category": "ANDA", "marketing_start_date": "20160426", "listing_expiration_date": "20261231"}