Package 68071-3675-2

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 68071-3675-2
Digits Only 6807136752
Product NDC 68071-3675
Product ID 68071-3675_20eb1df7-535e-a7bd-e063-6394a90ad98c
Description

20 TABLET, FILM COATED in 1 BOTTLE (68071-3675-2)

Marketing

Marketing Status
Marketed Since 2024-08-30
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": "20eb1df7-535e-a7bd-e063-6394a90ad98c", "openfda": {"upc": ["0368071367522"], "unii": ["804826J2HU"], "rxcui": ["308192"], "spl_set_id": ["20eb4ade-f3b8-db66-e063-6294a90ae846"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3675-2)", "package_ndc": "68071-3675-2", "marketing_start_date": "20240830"}], "brand_name": "Amoxicillin", "product_id": "68071-3675_20eb1df7-535e-a7bd-e063-6394a90ad98c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68071-3675", "generic_name": "Amoxicillin", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA065256", "marketing_category": "ANDA", "marketing_start_date": "20051109", "listing_expiration_date": "20261231"}