Package 42708-078-20

Brand: amoxicillin

Generic: amoxicillin
NDC Package Sample

Package Facts

Identity

Package NDC 42708-078-20
Digits Only 4270807820
Product NDC 42708-078
Product ID 42708-078_45867f6f-f9ed-c4aa-e063-6394a90a0cc3
Description

20 TABLET, FILM COATED in 1 BOTTLE (42708-078-20)

Marketing

Marketing Status
Marketed Since 2019-01-14
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": "45867f6f-f9ed-c4aa-e063-6394a90a0cc3", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["2700df91-c5ef-4931-9ad7-a3c1c146ccac"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "20 TABLET, FILM COATED in 1 BOTTLE (42708-078-20)", "package_ndc": "42708-078-20", "marketing_start_date": "20190114"}], "brand_name": "Amoxicillin", "product_id": "42708-078_45867f6f-f9ed-c4aa-e063-6394a90a0cc3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "42708-078", "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": "ANDA065256", "marketing_category": "ANDA", "marketing_start_date": "20051109", "listing_expiration_date": "20261231"}