Package 68788-8318-1
Brand: amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassiumPackage Facts
Identity
Package NDC
68788-8318-1
Digits Only
6878883181
Product NDC
68788-8318
Description
100 mL in 1 BOTTLE (68788-8318-1)
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": "2c966f10-3845-4fa9-aa1f-c56e7a671252", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617430"], "spl_set_id": ["618953a3-0256-42ce-9155-d35325f017aa"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-8318-1)", "package_ndc": "68788-8318-1", "marketing_start_date": "20221223"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68788-8318_2c966f10-3845-4fa9-aa1f-c56e7a671252", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68788-8318", "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": "400 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "57 mg/5mL"}], "application_number": "ANDA201090", "marketing_category": "ANDA", "marketing_start_date": "20221223", "listing_expiration_date": "20271231"}