Package 68788-7323-1

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 68788-7323-1
Digits Only 6878873231
Product NDC 68788-7323
Product ID 68788-7323_0aaa8a08-10ea-4b03-8734-13518addef54
Description

100 mL in 1 BOTTLE (68788-7323-1)

Marketing

Marketing Status
Marketed Since 2019-03-12
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": "0aaa8a08-10ea-4b03-8734-13518addef54", "openfda": {"unii": ["804826J2HU"], "rxcui": ["313850"], "spl_set_id": ["afef7c71-2d19-41ed-9213-b32ccc1bf1d3"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-7323-1)", "package_ndc": "68788-7323-1", "marketing_start_date": "20190312"}], "brand_name": "Amoxicillin", "product_id": "68788-7323_0aaa8a08-10ea-4b03-8734-13518addef54", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68788-7323", "generic_name": "Amoxicillin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "200 mg/5mL"}], "application_number": "ANDA065325", "marketing_category": "ANDA", "marketing_start_date": "20060619", "listing_expiration_date": "20271231"}