Terbinafine Hydrochloride
- Product NDC
- 37205-941
- 11-digit product format
- 372050941
- Labeler code
- 37205
- Product ID
- 37205-941_99993239-566c-4203-afc1-22c7438d4155
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Terbinafine Hydrochloride
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Cardinal Health
- Application
- ANDA077511
- Marketing category
- ANDA
- Marketing start
- 2007-07-02
- Marketing end
- 2020-05-31
- 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
FDA-Initiated Inactive NDC Indexing#