Package 68071-3716-2

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 68071-3716-2
Digits Only 6807137162
Product NDC 68071-3716
Description

20 TABLET, COATED in 1 BOTTLE (68071-3716-2)

Marketing

Marketing Status
Marketed Since 2024-11-06
Brand amoxicillin
Generic amoxicillin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2646715c-d336-9b32-e063-6394a90a120c", "openfda": {"upc": ["0368071371628"], "unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["26469497-14c2-adb2-e063-6394a90af30a"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (68071-3716-2)", "package_ndc": "68071-3716-2", "marketing_start_date": "20241106"}], "brand_name": "Amoxicillin", "product_id": "68071-3716_2646715c-d336-9b32-e063-6394a90a120c", "dosage_form": "TABLET, COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68071-3716", "generic_name": "Amoxicillin", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065255", "marketing_category": "ANDA", "marketing_start_date": "20060329", "listing_expiration_date": "20261231"}