Package 42571-164-47
Brand: amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassiumPackage Facts
Identity
Package NDC
42571-164-47
Digits Only
4257116447
Product NDC
42571-164
Description
100 mL in 1 BOTTLE (42571-164-47)
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": "22ff093e-19eb-7dd4-e063-6394a90ac20d", "openfda": {"upc": ["0342571163471"], "unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["617423", "617430"], "spl_set_id": ["8ea86ac2-174b-4da0-963f-6a051dccbe36"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (42571-164-47)", "package_ndc": "42571-164-47", "marketing_start_date": "20210701"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "42571-164_22ff093e-19eb-7dd4-e063-6394a90ac20d", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "42571-164", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Micro Labs Limited", "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": "ANDA205187", "marketing_category": "ANDA", "marketing_start_date": "20210701", "listing_expiration_date": "20261231"}