Package 72162-2211-2
Brand: amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassiumPackage Facts
Identity
Package NDC
72162-2211-2
Digits Only
7216222112
Product NDC
72162-2211
Description
20 TABLET, FILM COATED in 1 BOTTLE (72162-2211-2)
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": "11986a98-d463-4906-a6f0-21b8f001cc4e", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["917a76e9-eb2b-4d49-9418-ff919a73cfad"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (72162-2211-2)", "package_ndc": "72162-2211-2", "marketing_start_date": "20020314"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "72162-2211_11986a98-d463-4906-a6f0-21b8f001cc4e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "72162-2211", "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": "875 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA065063", "marketing_category": "ANDA", "marketing_start_date": "20020314", "listing_expiration_date": "20261231"}