Ethosuximide
- Product NDC
- 61748-024
- 11-digit product format
- 617480024
- Labeler code
- 61748
- Product ID
- 61748-024_fc97e367-f4f2-400d-8033-7f114fc03998
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethosuximide
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Versapharm Incorporated
- Application
- ANDA040506
- Marketing category
- ANDA
- Marketing start
- 2004-01-01
- Marketing end
- 0000-00-00
- Substance
- ETHOSUXIMIDE
- Active strength
- 250 mg/5mL
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 61748-024-16 | 61748002416 | 473 mL in 1 BOTTLE, PLASTIC (61748-024-16) | 473 ml | 2004-01-01 | 0000-00-00 | No | No | Current |