United States · FDA National Drug Code directory
Butenafine 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
- 79481-0086_5a993dc7-3490-c2a8-e063-6394a90a4637
- Product NDC
- 79481-0086
- Form
- CREAM
- Composition / generic term
- Butenafine Hydrochloride
- Labeler
- MEIJER DISTRIBUTION INC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231130
- Source listing expiry
- 20271231
Source-listed ingredients
- BUTENAFINE HYDROCHLORIDE — 10 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (79481-0086-1) / 30 g in 1 TUBE · 79481-0086-1
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →