Package 63187-542-00

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 63187-542-00
Digits Only 6318754200
Product NDC 63187-542
Description

100 mL in 1 BOTTLE (63187-542-00)

Marketing

Marketing Status
Marketed Since 2018-12-01
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": "51ae03ae-99b0-47e9-ae80-0e8e7b1fc7bc", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617423"], "spl_set_id": ["0f263ead-5be2-435e-9e5d-8f23fb1707e3"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (63187-542-00)", "package_ndc": "63187-542-00", "marketing_start_date": "20181201"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "63187-542_51ae03ae-99b0-47e9-ae80-0e8e7b1fc7bc", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "63187-542", "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": "200 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "28.5 mg/5mL"}], "application_number": "ANDA065098", "marketing_category": "ANDA", "marketing_start_date": "20040813", "listing_expiration_date": "20261231"}