Ivermectin
- Product NDC
- 63629-7275
- 11-digit product format
- 636297275
- Labeler code
- 63629
- Product ID
- 63629-7275_130bb860-3294-494c-8569-df64cf5ffc6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ivermectin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204154
- Marketing category
- ANDA
- Marketing start
- 2014-11-15
- Marketing end
- 0000-00-00
- Substance
- IVERMECTIN
- Active strength
- 3 mg/1
- Pharmacologic classes
- Antiparasitic [EPC],Pediculicide [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7275-1 | 63629727501 | 2 TABLET in 1 BOTTLE (63629-7275-1) | 2 tablet | 2017-05-11 | 0000-00-00 | No | No | Current |
| 63629-7275-2 | 63629727502 | 30 TABLET in 1 BOTTLE (63629-7275-2) | 30 tablet | 2017-05-11 | 0000-00-00 | No | No | Current |
| 63629-7275-3 | 63629727503 | 4 TABLET in 1 BOTTLE (63629-7275-3) | 4 tablet | 2017-05-11 | 0000-00-00 | No | No | Current |
| 63629-7275-4 | 63629727504 | 10 TABLET in 1 BOTTLE (63629-7275-4) | 10 tablet | 2017-05-11 | 0000-00-00 | No | No | Current |