Terbinafine Hydrochloride
- Product NDC
- 70518-0670
- 11-digit product format
- 705180670
- Labeler code
- 70518
- Product ID
- 70518-0670_8a9df3a5-e7fc-5da2-e053-2995a90a696b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Terbinafine Hydrochloride
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077511
- Marketing category
- ANDA
- Marketing start
- 2017-08-16
- 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