Package 70518-3886-0

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 70518-3886-0
Digits Only 7051838860
Product NDC 70518-3886
Product ID 70518-3886_3f8d44fe-be39-c260-e063-6294a90a7c23
Description

100 POUCH in 1 BOX (70518-3886-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3886-1)

Marketing

Marketing Status
Marketed Since 2023-10-05
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": "3f8d44fe-be39-c260-e063-6294a90a7c23", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308192"], "spl_set_id": ["f37eb415-77b2-41b0-8d20-64e821e4b05d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-3886-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-3886-1)", "package_ndc": "70518-3886-0", "marketing_start_date": "20231005"}], "brand_name": "Amoxicillin", "product_id": "70518-3886_3f8d44fe-be39-c260-e063-6294a90a7c23", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "70518-3886", "generic_name": "Amoxicillin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA065256", "marketing_category": "ANDA", "marketing_start_date": "20231005", "listing_expiration_date": "20261231"}