Trileptal

Product NDC

70518-1300

11-digit product format

705181300

Labeler code

70518

Product ID

70518-1300_91a0fbdb-0bfc-b8bd-e053-2995a90a1a5e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxcarbazepine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA021014

Marketing category

NDA

Marketing start

2018-07-12

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

2020-12-31

Current FDA listing

Historical FDA.report record