Virtual Medicinal Product (VMP) - Co-amoxiclav 500mg/100mg powder for solution for injection vials

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Name Details

Name Start Date End Date
Name Current Name Co-amoxiclav 500mg/100mg powder for solution for injection vials Start Date 18-05-2004 End Date
Previous Name Previous Name Co-amoxiclav 500mg/100mg injection vials Start Date 04-05-2004 End Date 17-05-2004
Abbreviated Name Abbreviated Name Co-amoxiclav 500mg/100mg inj vials Start Date 01-05-2009
Previous Abbreviated Name Co-amoxiclav 500mg/100mg pdr for soln for inj vials Previous Start Date 07-09-2004 Previous End Date 30-04-2009

Unit Dose & Form Information

DF Indicator
Discrete
UDFS Indicator
1
UDFS UOM
vial
Unit Dose UOM
vial

Summary

Prescribing Status
Valid as a prescribable product
Controlled Drug Category
No Controlled Drug Status
Route
Intravenous
Form
Powder for solution for injection
Ontology Form/Route
solutioninjection.intravenous, solutioninfusion.intravenous
Name Basis
BAN - British Approved Name

Codes

ATC Code
J01CR02
BNF Start Date End Date
Current BNF 05010103 Start Date 04-04-2022 End Date
Previous BNF 05010103 Start Date 01-02-2005 End Date 03-04-2022
SNOMED Codes
Code Start Date End Date
41947111000001102 09-06-2023
323567000 28-11-2002 08-06-2023

VMP Ingredients

VMP ingredients table
Name Basis of Strength Description BOSS Strength and UOM (Nmr) Strength and UOM (Dmr)
Amoxicillin sodium Based on Base Substance Amoxicillin 500 mg
Potassium clavulanate Based on Base Substance Clavulanic acid 100 mg

Parent Products

Virtual Medicinal Product Pack (VMPP) Information

Pack Size Drug Tariff Price Drug Tariff Payment Category
10 vial