Ethosuximide
- Product NDC
- 59762-2250
- 11-digit product format
- 597622250
- Labeler code
- 59762
- Product ID
- 59762-2250_2cdff9b3-e3df-4428-83ce-c72022e174e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethosuximide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA012380
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2015-10-12
- Marketing end
- 0000-00-00
- Substance
- ETHOSUXIMIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- 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 |
|---|
| 59762-2250-2 | 59762225002 | 100 CAPSULE in 1 BOTTLE (59762-2250-2) | 100 capsule | 2015-10-12 | 0000-00-00 | No | No | Current |