Package 71205-663-30

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 71205-663-30
Digits Only 7120566330
Product NDC 71205-663
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-663-30)

Marketing

Marketing Status
Marketed Since 2022-05-24
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": "787724dc-0b4b-4973-852e-c7d722f637b0", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0371205663902"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["787724dc-0b4b-4973-852e-c7d722f637b0"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-663-30)", "package_ndc": "71205-663-30", "marketing_start_date": "20220524"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-663-60)", "package_ndc": "71205-663-60", "marketing_start_date": "20220524"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-663-90)", "package_ndc": "71205-663-90", "marketing_start_date": "20220524"}], "brand_name": "Famotidine", "product_id": "71205-663_787724dc-0b4b-4973-852e-c7d722f637b0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "71205-663", "generic_name": "Famotidine", "labeler_name": "Proficient Rx LP", "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"}