Package 82804-017-12

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 82804-017-12
Digits Only 8280401712
Product NDC 82804-017
Description

125 mL in 1 BOTTLE (82804-017-12)

Marketing

Marketing Status
Marketed Since 2023-10-05
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": "e05caabb-b95c-4e54-890e-bbc371a20fc3", "openfda": {"upc": ["0382804017126"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["e05caabb-b95c-4e54-890e-bbc371a20fc3"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "125 mL in 1 BOTTLE (82804-017-12)", "package_ndc": "82804-017-12", "marketing_start_date": "20231005"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "82804-017_e05caabb-b95c-4e54-890e-bbc371a20fc3", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "82804-017", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "600 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "42.9 mg/5mL"}], "application_number": "ANDA201091", "marketing_category": "ANDA", "marketing_start_date": "20111220", "listing_expiration_date": "20261231"}