View the MUMFER registration information details.
Back to drug list
ItemsDrug Registration information
ID2531
No2531
Brand NameMUMFER
IngredientsIRON III HYDROXIDE POLYMALTOSE COMPLEX EQ.TO ELEMENTAL IRON 50MG/5ML
Dosage FormSYRUP
Primary PackagingBOTTLE
Storage
Shelf Life30 MONTHS
Pack Size150ML/BOTTLE/BOX
Dispensing Category
ATC Classification
Pharmaceutical Class
IndicationsTREATMENT OF LATENT IRON DEFICIENCY AND IRON DEFICIENCY ANAEMIA AND PREVENTION OF IRON DEFICIENCY BEFORE, DURING AND AFTER PREGNANCY.
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionBROWN COLOURED FLAVOURED LIQUID WITH SWEET TASTE.
Note
License OwnerVE PRODUCTS (LAO) CO.,LTD
ManufacturerGLENMARK PHARMACEUTICALS LIMITED
CountryINDIA
Import Registration No
Import Registration Date
ActivityCERTIFICATE RELEASED
Applied Date
FDD Registration No02 I 2753/06
FDD Registration Date30/01/2024
Expiry Date29/01/2027
Back to drug list
ADB ASEAN COVID-19 Laos JICA KOICA Global Fund WFP UHS Laos World Bank MOH Laos UNODC WHO SIDA