VIGABATRIN
- Product NDC
- 72158-101
- 11-digit product format
- 721580101
- Labeler code
- 72158
- Product ID
- 72158-101_ccf0e414-9225-4b41-8659-e292be7fa623
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VIGABATRIN
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Navisci Pte. Ltd.
- Application
- ANDA213390
- Marketing category
- ANDA
- Marketing start
- 2021-10-15
- Marketing end
- 0000-00-00
- Substance
- VIGABATRIN
- Active strength
- 500 mg/10mL
- Pharmacologic classes
- Anti-epileptic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 72158-101-50 | 72158010150 | 50 PACKET in 1 CARTON (72158-101-50) > 10 mL in 1 PACKET (72158-101-05) | 50 packet | 2021-10-15 | 0000-00-00 | No | No | Current |