View drug registration information details.
Items | Registration information |
ID | 137 |
No | 137 |
Brand Name | KAMZOLE 200 |
Ingredients | KETOCONAZOLE USP 200 MG |
Dosage Form | TABLELT |
Primary Packaging | ALU-ALU BLISTER |
Storage | STORE AT CONTROLLED ROOM TEMPERATURE 20 -25C |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 10 X 10'S |
Dispensing Category | PRESCRIPTION |
ATC Classification | - |
Pharmaceutical Class | ANTIFUNGAL |
Indications | TREATMENT FOR CANDIDIASIS, CHRONIC MUCOCUTANEOUS CANDIDIASIS, ORAL THRUSH CANDIDURIA, BLASTOMYCOSIS, COCCIDIOIMYCOSIS, HISTOPLASMOSIS, CHROMOMYCOSIS AND PARACOCCIDIOIDOMYCOSIS. FOR THE TREATMENT WITH SEVERE RECALCITRANT CUTANEOUS DERMATOPHYTE INFECTIONS |
Contraindications | DECREASED FUNCTION OF THE ADRENAL GLAND, VERY RAPID HEARTBEAT, PROLONGED QT INTERVAL ON EKG, ABNORMAL EKG WITH QT CHANGES FROM BIRTH, ABSENSCE OF STOMACH ACID, HEPATITIS CAUSED BY DRUGS, ABNORMAL LIVER FUNCTION TEST |
Side Effects | NAUSEA, HEADACHE, DIARRHEA, STOMACH PAIN, ABNORMAL LIVER FUNCTION TEST RESULT |
Unit Price | |
EDL |
Yes |
Description | WHITE, ROUND SHAPED, BICONVEX, UNCOATED TABLET, PLAIN ON BOTH SIDES OF EACH TABLET |
Note | |
License Owner | ASA LAO SOLE COMPANY LIMITED |
Manufacturer | IMPULSE PHARMA PVT.LTD |
Country | INDIA |
Import Registration No | KD/641 (FORM 25) |
Import Registration Date | 2019-11-26 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2025-02-24 |
FDD Registration No | 02 I 5189/22 |
FDD Registration Date | 2025-03-03 |
Expiry Date | 2030-03-02 |
Back to drug list
|