Vigabatrin
- Product NDC
- 16729-521
- 11-digit product format
- 167290521
- Labeler code
- 16729
- Product ID
- 16729-521_ecb6ac52-5414-bf6a-e053-2995a90a4ef2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vigabatrin
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Accord Healthcare Inc.
- Application
- ANDA214425
- Marketing category
- ANDA
- Marketing start
- 2021-04-28
- Marketing end
- 0000-00-00
- Substance
- VIGABATRIN
- Active strength
- 500 mg/1
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16729-521-11 | 16729052111 | 50 POWDER, FOR SOLUTION in 1 CARTON (16729-521-11) | 2021-04-28 | 0000-00-00 | No | No | Current |