Lamisil AT
- Product NDC
- 70518-1736
- 11-digit product format
- 705181736
- Labeler code
- 70518
- Product ID
- 70518-1736_96323da0-ae71-bb1c-e053-2995a90a218a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Terbinafine Hydrochloride
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077511
- Marketing category
- ANDA
- Marketing start
- 2018-12-15
- Marketing end
- 0000-00-00
- Substance
- TERBINAFINE HYDROCHLORIDE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record