Package 45865-230-20
Brand: amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassiumPackage Facts
Identity
Package NDC
45865-230-20
Digits Only
4586523020
Product NDC
45865-230
Description
20 TABLET, FILM COATED in 1 BOTTLE (45865-230-20)
Marketing
Marketing Status
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": "1275ba9e-689e-104c-e063-6394a90a2b15", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["1275ad58-c53f-20d0-e063-6394a90a4a43"], "manufacturer_name": ["Medsource Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (45865-230-20)", "package_ndc": "45865-230-20", "marketing_start_date": "20231130"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "45865-230_1275ba9e-689e-104c-e063-6394a90a2b15", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "45865-230", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Medsource Pharmaceuticals", "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": "ANDA205707", "marketing_category": "ANDA", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}