Vigabatrin
- Product NDC
- 64850-940
- 11-digit product format
- 648500940
- Labeler code
- 64850
- Product ID
- 64850-940_e5351b0d-e810-41f1-b56f-18245bbf43a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vigabatrin
- Dosage form
- FOR SOLUTION
- Route
- ORAL
- Labeler
- Elite Laboratories, Inc.
- Application
- ANDA214961
- Marketing category
- ANDA
- Marketing start
- 2022-06-24
- 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 |
|---|
| 64850-940-50 | 64850094050 | 50 PACKET in 1 CARTON (64850-940-50) > 10 mL in 1 PACKET (64850-940-01) | 50 packet | 2022-06-24 | 0000-00-00 | No | No | Current |