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RH073

Product Details
WHO Product ID
RH073
Status
Prequalified
INN, dosage form and strength
Magnesium sulphate Solution for injection 500mg/mL
Date of prequalification
Basis of listing
Prequalification - Abridged
Therapeutic area
Reproductive health
Type
Finished Pharmaceutical Product
Dosage form
Solution for injection
Reference authority
Medicines and Healthcare products Regulatory Agency (MHRA)
Applicant organization
Aurum Pharmaceuticals Ltd
Bampton Road, Harold Hill, Romford
Essex,
RM3 8UG
United Kingdom of Great Britain and Northern Ireland
Packaging details and storage conditions
Packaging Type
Ampoule, Neutral type I glass
Configuration
2mlx10
Shelf life (months)
36
Storage conditions
Do not store above 30°C
API Manufacturing Site(s)
By Organization
By Active Ingredient
K+S KALI GmbH
Werk Werra, Standort Hattorf, Hattorfer Strasse, 36269
Philippsthal (Werra),
Germany
Magnesium sulphate
Macco Organiques, S.R.O
Zahradni 1938/46c
Bruntál,
792 01
Czechia
Magnesium sulphate
FPP Manufacturing Site(s)
Macarthys Laboratories Limited
Bampton Road, Harold Hill, Romford
Essex,
RM3 8UG
United Kingdom of Great Britain and Northern Ireland
WHO Public Assessment Reports


Part 1 - Abstract
Part 2a - All accepted presentations
Part 2b - Visual appearance of the product
Part 3 - WHO-PQ recommended patient information leaflet*
Part 4 - WHO-PQ recommended summary of product characteristics*
Part 5 - Label
Part 6 - Discussion (status at the time of prequalification)
Part 7 - Steps before Prequalification
Part 8 - Steps following Prequalification (from 01 March 2014, only changes to the published information are included)

* This summary of product characteristics/patient information leaflet focus on uses of the medicine covered by WHO Prequalification Team - Medicines. The recommendations for use are based on WHO guidelines and on information from stringent regulatory authorities (term to be revised). The medicine may be authorised for additional or different uses by national medicines regulatory authorities. 

Samples of the artworks of the SPC/PIL/labelling have not been submitted. Therefore, control of compliance with WHOPAR guidelines (contents and format) has not been possible.

Part 1 , Part 2a , Part 2b , Part 5 , Part 7

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