Naftifine Hydrochloride
Active substance: naftifine
CREAM · NAFTIFINE HYDROCHLORIDE 10 mg/g
United StatesActive
Marketing holder: Sun Pharmaceutical Industries, Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- NAFTIFINE HYDROCHLORIDE · 10 mg/g
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-7085-7034-828e-bbbab6103c24,01a1208f-e5e8-7ce3-8e70-b958df9dac60,01a12091-24b2-72b3-a5e4-967e0dea4034,01a12096-2017-7555-8f86-8db639779c89,01a1209d-793d-78b2-af9b-7697c803f14a;count=5 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 51672-1362
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- TOPICAL
Sources
- product · openFDA NDC · 51672-1362 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 51672-1362 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 51672-1362 · Verified 2026-10-09 · open in source