Oxcarbazepine

Product NDC

0054-0099

11-digit product format

000540099

Labeler code

0054

Product ID

0054-0099_db7ab39d-577e-408a-8fb3-bdb3cf868664

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxcarbazepine

Dosage form

TABLET

Route

ORAL

Labeler

West-Ward Pharmaceticals Corp.

Application

ANDA077795

Marketing category

ANDA

Marketing start

2007-10-09

Marketing end

2020-08-23

Substance

OXCARBAZEPINE

Active strength

600 mg/1

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