ETHOSUXIMIDE
- Product NDC
- 71335-1763
- 11-digit product format
- 713351763
- Labeler code
- 71335
- Product ID
- 71335-1763_e7ddb61f-bc96-4106-ba63-111fd1773425
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ETHOSUXIMIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211928
- Marketing category
- ANDA
- Marketing start
- 2019-05-15
- 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
- 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 |
|---|
| 71335-1763-1 | 71335176301 | 90 CAPSULE in 1 BOTTLE (71335-1763-1) | 90 capsule | 2021-01-06 | 0000-00-00 | No | No | Current |