Tavaborole
- Product NDC
- 68180-958
- 11-digit product format
- 681800958
- Labeler code
- 68180
- Product ID
- 68180-958_fb25fb08-18e0-4a5a-881e-2ee67a3ddfab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tavaborole
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA212168
- Marketing category
- ANDA
- Marketing start
- 2021-07-09
- Marketing end
- 0000-00-00
- Substance
- TAVABOROLE
- Active strength
- 44 mg/mL
- Pharmacologic classes
- Oxaborole Antifungal [EPC],Protein Synthesis Inhibitors [MoA],Boron Compounds [CS]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68180-958-02 | 68180095802 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68180-958-02) > 10 mL in 1 BOTTLE, WITH APPLICATOR | 2021-05-31 | 0000-00-00 | No | No | Current |