Ethosuximide 00121-0670
Product NDC
00121-0670- Manufacturer
- Pai Holdings, Llc Dba Pai Pharma
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 22, 2000
- Listing Expires
- December 31, 2026
- Application
- ANDA040253
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ethosuximide | 250 mg/5mL |
Drug Class
Anti-epileptic Agent [EPC]Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(1)
473 mL in 1 BOTTLE (0121-0670-16)