Terbinafine Hydrochloride
- Product NDC
- 63629-8137
- 11-digit product format
- 636298137
- Labeler code
- 63629
- Product ID
- 63629-8137_42f6e2f8-7890-4129-b507-9489dc3844e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Terbinafine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077137
- Marketing category
- ANDA
- Marketing start
- 2014-08-13
- Marketing end
- 0000-00-00
- Substance
- TERBINAFINE HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Allylamine Antifungal [EPC], Allylamine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-8137-1 | 63629813701 | 30 TABLET in 1 BOTTLE (63629-8137-1) | 30 tablet | 2019-07-15 | 0000-00-00 | No | No | Current |