Ethosuximide

Product NDC

0093-9660

11-digit product format

000939660

Labeler code

0093

Product ID

0093-9660_ef2b9689-f74f-4904-b9df-bab0cdef2e62

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ethosuximide

Dosage form

SOLUTION

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA081306

Marketing category

ANDA

Marketing start

1994-07-01

Marketing end

2019-10-31

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

0000-00-00

Current FDA listing

Historical FDA.report record