United States · FDA National Drug Code directory
Terbinafine Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71205-127_ebcef20e-0991-4cd7-b79c-0d1a29b90fed
- Product NDC
- 71205-127
- Form
- TABLET
- Composition / generic term
- Terbinafine Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101227
- Source listing expiry
- 20261231
Source-listed ingredients
- TERBINAFINE HYDROCHLORIDE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET in 1 BOTTLE (71205-127-14) · 71205-127-14
- 15 TABLET in 1 BOTTLE (71205-127-15) · 71205-127-15
- 30 TABLET in 1 BOTTLE (71205-127-30) · 71205-127-30
- 35 TABLET in 1 BOTTLE (71205-127-35) · 71205-127-35
- 42 TABLET in 1 BOTTLE (71205-127-42) · 71205-127-42
- 45 TABLET in 1 BOTTLE (71205-127-45) · 71205-127-45
- 60 TABLET in 1 BOTTLE (71205-127-60) · 71205-127-60
- 90 TABLET in 1 BOTTLE (71205-127-90) · 71205-127-90
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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