Lamisil
- Product NDC
- 0067-3999
- 11-digit product format
- 000673999
- Labeler code
- 0067
- Product ID
- 0067-3999_331b6cb8-35ae-483d-be2e-350d6c565175
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TERBINAFINE HYDROCHLORIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- NDA020980
- Marketing category
- NDA
- Marketing start
- 2006-12-08
- Marketing end
- 0000-00-00
- Substance
- TERBINAFINE HYDROCHLORIDE
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 0067-3999-42 | 00067399942 | 1 TUBE in 1 CARTON (0067-3999-42) > 12 g in 1 TUBE | 1 tube | 2006-12-08 | 0000-00-00 | No | No | Current |