Package 68788-8759-1

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 68788-8759-1
Digits Only 6878887591
Product NDC 68788-8759
Product ID 68788-8759_4c858be1-f077-4602-b424-bf8b8c7d4da4
Description

150 mL in 1 BOTTLE (68788-8759-1)

Marketing

Marketing Status
Marketed Since 2024-10-17
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": "4c858be1-f077-4602-b424-bf8b8c7d4da4", "openfda": {"unii": ["804826J2HU"], "rxcui": ["239191"], "spl_set_id": ["0ce05282-995c-461e-b807-facb1fcbb405"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE (68788-8759-1)", "package_ndc": "68788-8759-1", "marketing_start_date": "20241017"}], "brand_name": "Amoxicillin", "product_id": "68788-8759_4c858be1-f077-4602-b424-bf8b8c7d4da4", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68788-8759", "generic_name": "Amoxicillin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/5mL"}], "application_number": "ANDA065322", "marketing_category": "ANDA", "marketing_start_date": "20241017", "listing_expiration_date": "20271231"}