Terbinafine Hydrochloride
- Product NDC
- 0536-1117
- 11-digit product format
- 005361117
- Labeler code
- 0536
- Product ID
- 0536-1117_0d3f2f7b-3be8-4d67-95f8-5adddc0f06e8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Terbinafine Hydrochloride
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Rugby Laboratories, Inc.
- Application
- ANDA077511
- Marketing category
- ANDA
- Marketing start
- 2007-07-02
- Marketing end
- 2020-09-30
- Substance
- TERBINAFINE HYDROCHLORIDE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record