Package 70518-4522-0

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 70518-4522-0
Digits Only 7051845220
Product NDC 70518-4522
Product ID 70518-4522_446cb28a-d04f-2873-e063-6394a90a94bd
Description

100 mL in 1 BOTTLE (70518-4522-0)

Marketing

Marketing Status
Marketed Since 2025-11-25
Brand amoxicillin
Generic amoxicillin
Sample Package No

Linked Drug Pages (1)

Amoxicillin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "446cb28a-d04f-2873-e063-6394a90a94bd", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308189"], "spl_set_id": ["2732a8c7-9e4b-43c9-9712-df4b237ab69c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (70518-4522-0)", "package_ndc": "70518-4522-0", "marketing_start_date": "20251125"}], "brand_name": "Amoxicillin", "product_id": "70518-4522_446cb28a-d04f-2873-e063-6394a90a94bd", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "70518-4522", "generic_name": "Amoxicillin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "400 mg/5mL"}], "application_number": "ANDA065334", "marketing_category": "ANDA", "marketing_start_date": "20251125", "listing_expiration_date": "20261231"}