Package 72162-2599-2

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 72162-2599-2
Digits Only 7216225992
Product NDC 72162-2599
Description

50 mL in 1 BOTTLE (72162-2599-2)

Marketing

Marketing Status
Marketed Since 2026-01-09
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": "3cf79dfc-32e4-4465-9aee-ac825817acd8", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310274"], "spl_set_id": ["900b4fd6-9c62-4b64-b4db-760c49ae0a42"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (72162-2599-2)", "package_ndc": "72162-2599-2", "marketing_start_date": "20260109"}], "brand_name": "FAMOTIDINE", "product_id": "72162-2599_3cf79dfc-32e4-4465-9aee-ac825817acd8", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "72162-2599", "generic_name": "FAMOTIDINE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FAMOTIDINE", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/5mL"}], "application_number": "ANDA217137", "marketing_category": "ANDA", "marketing_start_date": "20230810", "listing_expiration_date": "20271231"}