FDA
Terbinafine Hydrochloride
The FDA lists this product in 17 strengths and forms.
Composition
- Active ingredients
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE · TabletANDA076377-001 · Discontinued
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE · TabletANDA078229-001 · Discontinued
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE · TabletANDA077065-001 · Discontinued
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE · TabletANDA077195-001 · Discontinued
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE · TabletANDA077533-001 · Prescription
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE · TabletANDA077223-001 · Discontinued
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE · TabletThis page
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE · TabletANDA076390-001 · Prescription
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE · TabletANDA077137-001 · Prescription
- TERBINAFINE HYDROCHLORIDE EQ 250MG BASE · TabletANDA077136-001 · Discontinued
At a glance
- Brand name
- Terbinafine Hydrochloride
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Glenmark Pharms LTD
- Status
- Prescription
- FDA approval
- 2 Jul 2007
- Application
- ANDA078157-001