View the UTROGESTAN 200 MG registration information details.
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ItemsDrug Registration information
ID653
No653
Brand NameUTROGESTAN 200 MG
IngredientsPROGESTERONE MICRONIZED PH EUR 200 MG
Dosage FormSOFT CAPSULE, ORAL ROUTE
Primary PackagingALU-PVC BLISTER PACK
Storage
Shelf Life36 MONTHS
Pack SizeBOX OF 15'S
Dispensing Category
ATC Classification
Pharmaceutical Class
IndicationsDISORDERS ASSOCIATED WITH A PROGESTERONE DEFICIT IN PARTICULAR: PRE-MENSTRUAL SYNDROME, MENSTRUAL IRREGULARITIES DUE TO OVULATION DISORDERS OR ANOVULATION, BENIGN MASTOPATHY, PREMENOPAUSE, INFERTILITY CAUSED BY LUTEAL PHASE DEFECT, MENACE OF PRETERM DELIVERY
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionOVOID, SLIGHTLY YELLOW CAPSULE CONTAING A WHITISH OILY SUSPENSION
Note
License OwnerEXAMED CO.,LTD
ManufacturerCYNDEA PHARMA, S.L.
CountryBELGIUM
Import Registration No
Import Registration Date
ActivityCERTIFICATE RELEASED
Applied Date
FDD Registration No01 I 5170/22
FDD Registration Date25/10/2024
Expiry Date24/10/2029
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