Package 68645-140-59

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 68645-140-59
Digits Only 6864514059
Product NDC 68645-140
Product ID 68645-140_30161630-325a-4bb8-e063-6394a90a5e27
Description

60 TABLET, FILM COATED in 1 BOTTLE (68645-140-59)

Marketing

Marketing Status
Marketed Since 2009-10-26
Brand famotidine
Generic famotidine
Sample Package No

Linked Drug Pages (1)

Famotidine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "30161630-325a-4bb8-e063-6394a90a5e27", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0368645140599"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["f3abe0c2-2029-4d89-b413-606a421491e4"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68645-140-59)", "package_ndc": "68645-140-59", "marketing_start_date": "20091026"}], "brand_name": "Famotidine", "product_id": "68645-140_30161630-325a-4bb8-e063-6394a90a5e27", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "68645-140", "generic_name": "Famotidine", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA075511", "marketing_category": "ANDA", "marketing_start_date": "20091026", "listing_expiration_date": "20261231"}