VIGADRONE
- Product NDC
- 73289-0002
- 11-digit product format
- 732890002
- Labeler code
- 73289
- Product ID
- 73289-0002_edae8af2-402e-0afd-e053-2995a90aded1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vigabatrin
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Aucta Pharmaceuticals, Inc.
- Application
- ANDA210196
- Marketing category
- ANDA
- Marketing start
- 2018-06-21
- Marketing end
- 0000-00-00
- Substance
- VIGABATRIN
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Anti-epileptic Agent [EPC]
- 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 |
|---|
| 73289-0002-0 | 73289000200 | 50 PACKAGE in 1 CARTON (73289-0002-0) > 10 mL in 1 PACKAGE | 50 package | 2018-06-21 | 0000-00-00 | No | No | Current |