Package 55289-845-21
Brand: amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassiumPackage Facts
Identity
Package NDC
55289-845-21
Digits Only
5528984521
Product NDC
55289-845
Description
21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-845-21)
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": "419b7d75-b6cc-e646-e063-6294a90a8d2e", "openfda": {"upc": ["0355289845201"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["cc445a39-d84c-4b76-9fb8-ae302e7cd96b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-845-06)", "package_ndc": "55289-845-06", "marketing_start_date": "20121206"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-845-20)", "package_ndc": "55289-845-20", "marketing_start_date": "20121206"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-845-21)", "package_ndc": "55289-845-21", "marketing_start_date": "20121206"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-845-28)", "package_ndc": "55289-845-28", "marketing_start_date": "20121206"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-845-30)", "package_ndc": "55289-845-30", "marketing_start_date": "20121206"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "55289-845_419b7d75-b6cc-e646-e063-6294a90a8d2e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "55289-845", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "ANDA065101", "marketing_category": "ANDA", "marketing_start_date": "20021031", "listing_expiration_date": "20261231"}