Package 70518-2333-0

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 70518-2333-0
Digits Only 7051823330
Product NDC 70518-2333
Product ID 70518-2333_4a02c696-4b58-6767-e063-6394a90ad645
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2333-0)

Marketing

Marketing Status
Marketed Since 2019-10-01
Brand amoxicillin
Generic amoxicillin
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a02c696-4b58-6767-e063-6394a90ad645", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["a2c91cf0-a4e4-44c0-b712-bee63dd6c22b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2333-0)", "package_ndc": "70518-2333-0", "marketing_start_date": "20191001"}], "brand_name": "Amoxicillin", "product_id": "70518-2333_4a02c696-4b58-6767-e063-6394a90ad645", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "70518-2333", "generic_name": "Amoxicillin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065256", "marketing_category": "ANDA", "marketing_start_date": "20191001", "listing_expiration_date": "20271231"}