Package 72162-2210-2

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 72162-2210-2
Digits Only 7216222102
Product NDC 72162-2210
Description

20 TABLET, FILM COATED in 1 BOTTLE (72162-2210-2)

Marketing

Marketing Status
Marketed Since 2002-03-15
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": "cef7f4b1-d750-4f09-aa7a-25afaf2020d5", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["71812ac4-9264-49f2-b9ab-ea1efd1af452"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (72162-2210-2)", "package_ndc": "72162-2210-2", "marketing_start_date": "20020315"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "72162-2210_cef7f4b1-d750-4f09-aa7a-25afaf2020d5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "72162-2210", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA065064", "marketing_category": "ANDA", "marketing_start_date": "20020315", "listing_expiration_date": "20261231"}