LAMISIL
Google image searchProduct monograph
Active ingredient
terbinafine hydrochloride, 1 %/W/W
DIN: 02238703
Dosage form(s): SPRAY
Route(s) of administration: TOPICAL
Schedule: Prescription
Company: NOVARTIS PHARMACEUTICALS CANADA INC
Date: 05-JAN-1999
ATC:
- D01 — ANTIFUNGALS FOR DERMATOLOGICAL USE (ATC, ATC/DDD, )
- D01A — ANTIFUNGALS FOR TOPICAL USE (ATC, ATC/DDD)
- D01AE — Other antifungals for topical use (ATC, ATC/DDD)
- D01AE15 — TERBINAFINE (ATC/DDD)
Reference brand drug: Lamisil
Pharmaceutical standard: MFR
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Novartis Pharmaceuticals Canada Inc
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