Package 68788-8852-1

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 68788-8852-1
Digits Only 6878888521
Product NDC 68788-8852
Product ID 68788-8852_992d7829-34d1-4c88-8a5c-1a92d001d194
Description

100 mL in 1 BOTTLE (68788-8852-1)

Marketing

Marketing Status
Marketed Since 2025-03-24
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": "992d7829-34d1-4c88-8a5c-1a92d001d194", "openfda": {"unii": ["804826J2HU"], "rxcui": ["313850"], "spl_set_id": ["992d7829-34d1-4c88-8a5c-1a92d001d194"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-8852-1)", "package_ndc": "68788-8852-1", "marketing_start_date": "20250324"}], "brand_name": "Amoxicillin", "product_id": "68788-8852_992d7829-34d1-4c88-8a5c-1a92d001d194", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68788-8852", "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": "20250324", "listing_expiration_date": "20261231"}