View the OLAVEX 5 MD registration information details.
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ItemsDrug Registration information
ID2537
No2537
Brand NameOLAVEX 5 MD
IngredientsOlanzapine USP 5 mg
Dosage FormTablets
Primary PackagingAlu-Alu Blister
Storage
Shelf Life3 YEARS
Pack SizeBOX OF 3 X 10'S
Dispensing Category
ATC Classification
Pharmaceutical Class
Indicationsfor the treatment of schizophrenia, for the treatment of moderate to severe manic episode, In patients whose manic episode has responded to OLAVEX treatment, OLAVEX is indicated for the prevention of recurrence in patients with bipolar disorder
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionYellow colour round shape flate uncoated tablet with Breakline on one side.
Note
License OwnerVE PRODUCTS (LAO) CO.,LTD
ManufacturerWEST-COAST PHARMACEUTICAL WORKS LTD
CountryINDIA
Import Registration No
Import Registration Date
ActivityCERTIFICATE RELEASED
Applied Date
FDD Registration No12 I 5837/24
FDD Registration Date30/12/2024
Expiry Date29/12/2029
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