Package 70518-4395-0

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 70518-4395-0
Digits Only 7051843950
Product NDC 70518-4395
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4395-0)

Marketing

Marketing Status
Marketed Since 2025-07-21
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": "3a6f9273-40ae-91f5-e063-6294a90a852c", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["8dbf43e0-856f-443b-b8a4-c69e006878ea"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4395-0)", "package_ndc": "70518-4395-0", "marketing_start_date": "20250721"}], "brand_name": "Famotidine", "product_id": "70518-4395_3a6f9273-40ae-91f5-e063-6294a90a852c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "70518-4395", "generic_name": "Famotidine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA217400", "marketing_category": "ANDA", "marketing_start_date": "20250721", "listing_expiration_date": "20261231"}