VIGABATRIN
- Product NDC
- 0574-0201
- 11-digit product format
- 005740201
- Labeler code
- 0574
- Product ID
- 0574-0201_05bc949b-e493-4379-a134-a000d134cf22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vigabatrin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Padagis US LLC
- Application
- ANDA215109
- Marketing category
- ANDA
- Marketing start
- 2022-06-29
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0574-0201-01 | 00574020101 | 100 TABLET in 1 BOTTLE (0574-0201-01) | 100 tablet | 2022-06-29 | 0000-00-00 | No | No | Current |