Registered Uganda · NDA

MOXIFLOXACIN HYDROCHLORIDE

NDA/MAL/HDP/7364 ORAL SOLID ORDINARY FILM-COATED TABLETS 400MG

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Registration & product details

Registration no.
NDA/MAL/HDP/7364
Registration date
01/07/2017
Expiry date
-
Status
Registered
Active ingredient
-
Dosage form
ORAL SOLID ORDINARY FILM-COATED TABLETS
Strength
400MG
Pack size
1.0X7.0 TABLET BLISTER, 1.0X7.0 X15.0 TABLET BLISTER
Therapeutic class
-
Manufacturer / MAH
?lko ?laç Sanayi Ve Ticaret A. ?-3. Organize Sanayi Bölgesi Kuddusi Cad. 23. Sok. No:1selçuklu / Konya |
Applicant / LTR
?LKO ?LAÇ SANAYI VE TICARET A. ?.
Country of origin
TURKEY |
Manufacturer location
Rings Rezidans, Veysel Karani, Çolakoğlu Sokağı No: 10 Kat: 7-8-9, 34885 Sancaktepe/İstanbul, Türkiye

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

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