Package 0143-9982-50

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 0143-9982-50
Digits Only 0143998250
Product NDC 0143-9982
Description

50 mL in 1 BOTTLE (0143-9982-50)

Marketing

Marketing Status
Marketed Since 2007-12-01
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": "d26c7880-d893-458e-8cc9-327a8ad2d7df", "openfda": {"nui": ["N0000175930", "N0000000202"], "upc": ["0301439981015", "0301439982012"], "unii": ["804826J2HU", "23521W1S24"], "rxcui": ["617423", "617430"], "spl_set_id": ["240bcdcb-31d9-40a0-87e1-bd16264a2e20"], "pharm_class_epc": ["beta Lactamase Inhibitor [EPC]"], "pharm_class_moa": ["beta Lactamase Inhibitors [MoA]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (0143-9982-01)", "package_ndc": "0143-9982-01", "marketing_start_date": "20071201"}, {"sample": false, "description": "50 mL in 1 BOTTLE (0143-9982-50)", "package_ndc": "0143-9982-50", "marketing_start_date": "20071201"}, {"sample": false, "description": "75 mL in 1 BOTTLE (0143-9982-75)", "package_ndc": "0143-9982-75", "marketing_start_date": "20071201"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "0143-9982_d26c7880-d893-458e-8cc9-327a8ad2d7df", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "0143-9982", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "400 mg/5mL"}, {"name": "CLAVULANIC ACID", "strength": "57 mg/5mL"}], "application_number": "ANDA065191", "marketing_category": "ANDA", "marketing_start_date": "20071201", "listing_expiration_date": "20261231"}