Package 68788-8317-2
Brand: amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassiumPackage Facts
Identity
Package NDC
68788-8317-2
Digits Only
6878883172
Product NDC
68788-8317
Description
20 TABLET, FILM COATED in 1 BOTTLE (68788-8317-2)
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": "95ca3695-cb4f-4ce9-8f68-a22e2d72d17c", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["d23b6952-5e4c-4103-9fe0-a916b1e2e1b9"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-8317-2)", "package_ndc": "68788-8317-2", "marketing_start_date": "20221223"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68788-8317_95ca3695-cb4f-4ce9-8f68-a22e2d72d17c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68788-8317", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Preferred 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": "ANDA091569", "marketing_category": "ANDA", "marketing_start_date": "20221223", "listing_expiration_date": "20271231"}