Moxidectin
- Product NDC
- 71705-051
- 11-digit product format
- 717050051
- Labeler code
- 71705
- Product ID
- 71705-051_d506c256-d6b7-0a58-e053-2995a90ae660
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxidectin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Medicines Development for Global Health
- Application
- NDA210867
- Marketing category
- NDA
- Marketing start
- 2019-12-02
- Marketing end
- 0000-00-00
- Substance
- MOXIDECTIN
- Active strength
- 2 mg/1
- 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 |
|---|
| 71705-051-01 | 71705005101 | 500 TABLET in 1 BOTTLE, PLASTIC (71705-051-01) | 500 tablet | 2019-12-02 | 0000-00-00 | No | No | Current |