
USFDA APPLICATION NUMBER - 22071 / DOSAGE - GRANULE;ORAL - EQ 187.5MG BASE/PACKET
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| TERBINAFINE HYDROCHLORIDE(UNII: 012C11ZU6G) (TERBINAFINE - UNII:G7RIW8S0XP) | TERBINAFINE | 125mg | 187.5mg |
Inactive Ingredients
| Ingredient Name | Novartis Pharmaceuticals Corporation |
|---|---|
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |
| DIBUTYL SEBACATE(4W5IH7FLNY) | |
| HYPROMELLOSES(3NXW29V3WO) | |
| MAGNESIUM STEARATE(70097M6I30) | |
| NITROGEN(N762921K75) | |
| POLYETHYLENE GLYCOLS(3WJQ0SDW1A) | |
| SILICON DIOXIDE(ETJ7Z6XBU4) | |
| SODIUM LAURYL SULFATE(368GB5141J) | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) |