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Logo PULMAX 100 MDI

For full prescribing information refer to the package insert approved by the medicines regulatory authority.

SCHEDULING STATUS:
no data

PROPRIETARY NAME
(and dosage form):

PULMAX 100 MDI
dry powder for inhalation

COMPOSITION:
Each actuation contains
budesonide 100.0 micrograms

ATC CLASSIFICATION:
no data

PRESENTATION/PACK SIZE:
no data

REGISTRATION NUMBER:
37/21.5.1/0013

APPLICANT:
BIOTECH LABORATORIES (PTY) LTD
http://www.biotech.co.za/

MANUFACTURER:
NORTON (WATERFORD) LIMITED, WATERFORD, IRELAND

AVAILABILITY:
no data

DATE OF REGISTRATION:
05 December 2013

SOURCE: Government Gazette -
STAATSKOERANT, 13 JUNIE 2014 No. 37727
NOTICE 405 OF 2014 - MEDICINES CONTROL COUNCIL

Date posted: July 2014

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