Lamisil AT
- Product NDC
- 0067-8114
- 11-digit product format
- 000678114
- Labeler code
- 0067
- Product ID
- 0067-8114_e076139d-60e6-4e93-81b0-aacebf68cbfb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Terbinafine Hydrochloride
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- ANDA077511
- Marketing category
- ANDA
- Marketing start
- 2007-07-02
- Marketing end
- 0000-00-00
- Substance
- TERBINAFINE HYDROCHLORIDE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0067-8114-12 | 00067811412 | 1 TUBE in 1 CARTON (0067-8114-12) > 12 g in 1 TUBE | 1 tube | 2007-07-02 | 0000-00-00 | No | No | Current |