Lamisil - terbinafine hydrochloride
Navigation: NDC > Supplier starting with: N > NOVARTIS PHARMACEUTICALS CORPORATION| Field | Value |
|---|---|
| NDC Code: | 0078-0179 |
| Proprietary Name: | Lamisil |
| Suffix: | |
| Non-Proprietary Name: | terbinafine hydrochloride |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 10-05-1996 |
| Category Name: | NDA |
| Application Number: | NDA020539 |
| Labeler: | NOVARTIS PHARMACEUTICALS CORPORATION |
| Substance Name: | TERBINAFINE HYDROCHLORIDE |
| Active Numerator Strength: | 250 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC] |
| DEA Schedule: |