Oxcarbazepine

Product NDC

50090-2573

11-digit product format

500902573

Labeler code

50090

Product ID

50090-2573_b187c8d9-6856-4028-89d3-d4801b109457

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxcarbazepine

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA077795

Marketing category

ANDA

Marketing start

2007-10-09

Marketing end

0000-00-00

Substance

OXCARBAZEPINE

Active strength

300 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record