Tavaborole
- Product NDC
- 63629-8704
- 11-digit product format
- 636298704
- Labeler code
- 63629
- Product ID
- 63629-8704_1ed32bb5-840c-46e6-9d23-327cf9f6d075
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tavaborole
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211848
- Marketing category
- ANDA
- Marketing start
- 2021-01-10
- Marketing end
- 0000-00-00
- Substance
- TAVABOROLE
- Active strength
- 44 mg/mL
- Pharmacologic classes
- Boron Compounds [CS], Oxaborole Antifungal [EPC], Protein Synthesis Inhibitors [MoA]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8704-1 | 63629870401 | 1 BOTTLE, GLASS in 1 CARTON (63629-8704-1) > 10 mL in 1 BOTTLE, GLASS | 2021-01-10 | 0000-00-00 | No | No | Current |