Package 82868-067-14
Brand: amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassiumPackage Facts
Identity
Package NDC
82868-067-14
Digits Only
8286806714
Product NDC
82868-067
Description
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-067-14)
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": "47aa03bc-feaf-be55-e063-6394a90a656d", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["26e1d503-ab8b-ca85-e063-6394a90aaae3"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-067-14)", "package_ndc": "82868-067-14", "marketing_start_date": "20241017"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "82868-067_47aa03bc-feaf-be55-e063-6394a90a656d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "82868-067", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Northwind Health Company, LLC", "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": "ANDA091568", "marketing_category": "ANDA", "marketing_start_date": "20241017", "listing_expiration_date": "20271231"}