Package 0527-5190-80

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 0527-5190-80
Digits Only 0527519080
Product NDC 0527-5190
Description

55 mL in 1 BOTTLE (0527-5190-80)

Marketing

Marketing Status
Marketed Since 2025-06-02
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": "4aedf984-0009-404b-8c21-8af5f225f9db", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310274"], "spl_set_id": ["7e0da8be-b001-400e-99d1-37f335b1d7b3"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "55 mL in 1 BOTTLE (0527-5190-80)", "package_ndc": "0527-5190-80", "marketing_start_date": "20250602"}], "brand_name": "Famotidine", "product_id": "0527-5190_4aedf984-0009-404b-8c21-8af5f225f9db", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0527-5190", "generic_name": "Famotidine", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/5mL"}], "application_number": "ANDA217982", "marketing_category": "ANDA", "marketing_start_date": "20250602", "listing_expiration_date": "20261231"}