Lamisil AT
- Product NDC
- 84485-3606
- 11-digit product format
- 844853606
- Labeler code
- 84485
- Product ID
- 84485-3606_d3e75665-e2d4-47d9-baaa-93817b5fbf00
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- terbinafine hydrochloride
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Karo Healthcare Inc.
- Application
- NDA021124
- Marketing category
- NDA
- Marketing start
- 2025-12-10
- Substance
- TERBINAFINE HYDROCHLORIDE
- Active strength
- 1 g/100g
- Pharmacologic classes
- Allylamine Antifungal [EPC], Allylamine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lamisil AT
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TERBINAFINE HYDROCHLORIDE | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 012C11ZU6G |
| Rxcui | 992535, 992536 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84485-3606-4 | Lamisil AT | 120 g in 1 CAN | SPRAY | 120 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84485-3606-4 | 84485360604 | 120 g in 1 CAN (84485-3606-4) | 120 g | 2025-12-10 | No | No | Historical |