Package 50090-6222-0

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 50090-6222-0
Digits Only 5009062220
Product NDC 50090-6222
Description

100 mL in 1 BOTTLE (50090-6222-0)

Marketing

Marketing Status
Marketed Since 2022-11-11
Brand amoxicillin and clavulanate potassium
Generic amoxicillin and clavulanate potassium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cb8142e-02a7-4914-baaa-9f943a11fccc", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617423"], "spl_set_id": ["61f9224b-a91b-4154-a7f3-22c14601230f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (50090-6222-0)", "package_ndc": "50090-6222-0", "marketing_start_date": "20221111"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "50090-6222_2cb8142e-02a7-4914-baaa-9f943a11fccc", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "50090-6222", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "200 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "28.5 mg/5mL"}], "application_number": "ANDA201090", "marketing_category": "ANDA", "marketing_start_date": "20111220", "listing_expiration_date": "20261231"}