Package 68071-3822-3

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 68071-3822-3
Digits Only 6807138223
Product NDC 68071-3822
Description

3 TABLET, FILM COATED in 1 BOTTLE (68071-3822-3)

Marketing

Marketing Status
Marketed Since 2025-04-02
Brand amoxicillin and clavulanate potassium
Generic amoxicillin and clavulanate potassium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31d00834-4ab4-d764-e063-6294a90ab395", "openfda": {"upc": ["0368071382235"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["31d00820-1c20-d52b-e063-6394a90ac312"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (68071-3822-3)", "package_ndc": "68071-3822-3", "marketing_start_date": "20250402"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68071-3822_31d00834-4ab4-d764-e063-6294a90ab395", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68071-3822", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA065063", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}