Package 72789-418-14
Brand: amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassiumPackage Facts
Identity
Package NDC
72789-418-14
Digits Only
7278941814
Product NDC
72789-418
Description
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-418-14)
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": "41238c5b-65fc-6526-e063-6394a90ac11c", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["0425932a-f6e1-49a6-8480-720f179ace14"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-418-14)", "package_ndc": "72789-418-14", "marketing_start_date": "20240703"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "72789-418_41238c5b-65fc-6526-e063-6394a90ac11c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "72789-418", "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"}