Registered Uganda · NDA

APREMILAST

NDA/MAL/HDP/10797 ORAL SOLID ORDINARY FILM-COATED TABLETS 10MG TABLETS CO-PACKED WITH 20MG TABLETS AND 30MG TABLETS

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Registration & product details

Registration no.
NDA/MAL/HDP/10797
Registration date
25/05/2023
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
ORAL SOLID ORDINARY FILM-COATED TABLETS
Strength
10MG TABLETS CO-PACKED WITH 20MG TABLETS AND 30MG TABLETS
Pack size
1.0X1.0 CARTON CARTON [4*10MG CO-PACKED WITH 4*20MG CO-PACKED WITH 19*30MG TABLETS],1.0X1.0 CARTON CARTON [4*10MG CO-PACKED WITH 4*20MG CO-PACKED WITH 47*30MG TABLETS]
Therapeutic class
-
Manufacturer / MAH
Glenmark Pharmaceuticals Limited
Applicant / LTR
GLENMARK PHARMACEUTICALS LTD
Country of origin
INDIA
Manufacturer location
Plot No.2, Phase II, Pharma Zone, ISEZ, Pithampur Industrial Area, Pithampur, Kalibillod, Madhya Pradesh 454774, India

Source: National Drug Authority · fetched 2026-04-21 17:37:05 · updated 2026-09-12 04:00:20

Disclaimer: This information is sourced from National Drug Authority (Uganda). Always consult a qualified healthcare professional before using any medication.