Package 83324-139-30

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 83324-139-30
Digits Only 8332413930
Product NDC 83324-139
Description

1 BOTTLE in 1 CARTON (83324-139-30) / 30 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-11-01
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": "9052e30a-9722-1394-0309-e0a11ecf9ec0", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["199047", "310273"], "spl_set_id": ["7fbc5e10-30c6-7f8d-1040-d48a80fe4d79"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Chain Drug Marketing Association INC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (83324-139-30)  / 30 TABLET in 1 BOTTLE", "package_ndc": "83324-139-30", "marketing_start_date": "20251101"}], "brand_name": "Famotidine", "product_id": "83324-139_9052e30a-9722-1394-0309-e0a11ecf9ec0", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "83324-139", "generic_name": "Famotidine", "labeler_name": "Chain Drug Marketing Association INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "10 mg/1"}], "application_number": "ANDA077367", "marketing_category": "ANDA", "marketing_start_date": "20251101", "listing_expiration_date": "20261231"}