Package 68788-7414-2

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 68788-7414-2
Digits Only 6878874142
Product NDC 68788-7414
Product ID 68788-7414_2c9fcee1-fa3e-4ac1-ad88-41c3cff5a2a1
Description

20 TABLET, FILM COATED in 1 BOTTLE (68788-7414-2)

Marketing

Marketing Status
Marketed Since 2020-03-25
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": "2c9fcee1-fa3e-4ac1-ad88-41c3cff5a2a1", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["4b23e6f5-9287-4c01-b795-b8c538833039"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-7414-2)", "package_ndc": "68788-7414-2", "marketing_start_date": "20200325"}], "brand_name": "Amoxicillin", "product_id": "68788-7414_2c9fcee1-fa3e-4ac1-ad88-41c3cff5a2a1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68788-7414", "generic_name": "Amoxicillin", "labeler_name": "Preferred Pharmaceuticals 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": "20200325", "listing_expiration_date": "20271231"}