Ivermectin
- Product NDC
- 51672-4211
- 11-digit product format
- 516724211
- Labeler code
- 51672
- Product ID
- 51672-4211_92921d55-1976-4d38-8e19-5c1705f052b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ivermectin
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Taro Pharmaceuticals U.S.A., Inc.
- Application
- ANDA210720
- Marketing category
- ANDA
- Marketing start
- 2020-05-06
- Marketing end
- 0000-00-00
- Substance
- IVERMECTIN
- Active strength
- 5 mg/g
- Pharmacologic classes
- Antiparasitic [EPC],Pediculicide [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 51672-4211-8 | 51672421108 | 1 TUBE in 1 CARTON (51672-4211-8) > 117 g in 1 TUBE | 1 tube | 2020-05-06 | 0000-00-00 | No | No | Current |