Oxcarbazepine

Product NDC

68788-7306

11-digit product format

687887306

Labeler code

68788

Product ID

68788-7306_45e95a1c-e602-493c-8401-3570f7922bed

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxcarbazepine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA077794

Marketing category

ANDA

Marketing start

2019-01-03

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record