TAVABOROLE
- Product NDC
- 71589-010
- 11-digit product format
- 715890010
- Labeler code
- 71589
- Product ID
- 71589-010_46430cca-61e0-43ed-a2d0-6ae8a8871f80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TAVABOROLE
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Aleor Dermaceuticals Limited
- Application
- ANDA212188
- Marketing category
- ANDA
- Marketing start
- 2020-10-23
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71589-010-04 | 71589001004 | 1 BOTTLE, DROPPER in 1 CARTON (71589-010-04) > 4 mL in 1 BOTTLE, DROPPER | 2020-10-23 | 0000-00-00 | No | No | Current |
| 71589-010-10 | 71589001010 | 1 BOTTLE, DROPPER in 1 CARTON (71589-010-10) > 10 mL in 1 BOTTLE, DROPPER | 2020-10-23 | 0000-00-00 | No | No | Current |