Package 42708-112-20

Brand: amoxicillin

Generic: amoxicillin
NDC Package Sample

Package Facts

Identity

Package NDC 42708-112-20
Digits Only 4270811220
Product NDC 42708-112
Product ID 42708-112_4682c86c-a853-ade0-e063-6394a90acbce
Description

20 TABLET, FILM COATED in 1 BOTTLE (42708-112-20)

Marketing

Marketing Status
Marketed Since 2018-04-17
Brand amoxicillin
Generic amoxicillin
Sample Package Yes

Linked Drug Pages (1)

Amoxicillin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4682c86c-a853-ade0-e063-6394a90acbce", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["7f40b439-d826-4a19-b184-702e9bd5a883"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "20 TABLET, FILM COATED in 1 BOTTLE (42708-112-20)", "package_ndc": "42708-112-20", "marketing_start_date": "20180417"}], "brand_name": "Amoxicillin", "product_id": "42708-112_4682c86c-a853-ade0-e063-6394a90acbce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "42708-112", "generic_name": "Amoxicillin", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065056", "marketing_category": "ANDA", "marketing_start_date": "20000926", "listing_expiration_date": "20261231"}