Oxcarbazepine

Product NDC

55700-569

11-digit product format

557000569

Labeler code

55700

Product ID

55700-569_972b37f5-c2a0-4d01-815f-99562880e7de

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxcarbazepine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA077802

Marketing category

ANDA

Marketing start

2017-12-21

Marketing end

0000-00-00

Substance

OXCARBAZEPINE

Active strength

150 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