Package 72205-233-84

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 72205-233-84
Digits Only 7220523384
Product NDC 72205-233
Description

55 mL in 1 BOTTLE (72205-233-84)

Marketing

Marketing Status
Marketed Since 2025-08-16
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": "21953598-e7ec-45c2-8fca-05550a1ddf38", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310274"], "spl_set_id": ["21953598-e7ec-45c2-8fca-05550a1ddf38"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "55 mL in 1 BOTTLE (72205-233-84)", "package_ndc": "72205-233-84", "marketing_start_date": "20250816"}], "brand_name": "FAMOTIDINE", "product_id": "72205-233_21953598-e7ec-45c2-8fca-05550a1ddf38", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "72205-233", "generic_name": "FAMOTIDINE", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FAMOTIDINE", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/5mL"}], "application_number": "ANDA219863", "marketing_category": "ANDA", "marketing_start_date": "20250724", "listing_expiration_date": "20261231"}