LAMISIL
Identification of Lamisil
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Active ingredient
terbinafine (terbinafine hydrochloride), 250 MG
DIN: 02031116
Dosage form(s): TABLET
Route(s) of administration: ORAL
Schedule: Prescription
Company: NOVARTIS PHARMACEUTICALS CANADA INC
Date: 23-FEB-1999
ATC:
- D01 — ANTIFUNGALS FOR DERMATOLOGICAL USE (ATC, ATC/DDD, )
- D01B — ANTIFUNGALS FOR SYSTEMIC USE (ATC, ATC/DDD)
- D01BA — Antifungals for systemic use (ATC, ATC/DDD)
- D01BA02 — TERBINAFINE (ATC/DDD)
Reference brand drug: Lamisil
Pharmaceutical standard: MFR
External Links for Lamisil
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Novartis Pharmaceuticals Canada Inc
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