Package 70518-3676-2
Brand: amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassiumPackage Facts
Identity
Package NDC
70518-3676-2
Digits Only
7051836762
Product NDC
70518-3676
Description
28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3676-2)
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": "3f27f3bb-3c09-3fab-e063-6394a90a0cb5", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["80bef3fd-4f6f-4190-8865-9ac46c8947a3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3676-2)", "package_ndc": "70518-3676-2", "marketing_start_date": "20250618"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "70518-3676_3f27f3bb-3c09-3fab-e063-6394a90a0cb5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "70518-3676", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "REMEDYREPACK INC.", "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": "20230315", "listing_expiration_date": "20261231"}