NDC 68999-064 – Ethosuximide

Ethosuximide 250 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC68999-064

Product details

Brand name
Ethosuximide
Generic name
Ethosuximide
Labeler
Chartwell Governmental & Specialty RX, LLC.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA040506
Marketed since
December 22, 2003
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Ethosuximide →

Package NDC codes (1)

Package NDCDescriptionSince
68999-064-242 TRAY in 1 BOX (68999-064-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-064-05)Jun 9, 2026

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