Trezix

Product NDC

66992-340

11-digit product format

669920340

Labeler code

66992

Product ID

66992-340_e87737f3-85f9-4e86-b66a-a59765b77611

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

acetaminophen, caffeine, dihydrocodeine bitartrate

Dosage form

CAPSULE

Route

ORAL

Labeler

WraSer LLC

Application

ANDA040688

Marketing category

ANDA

Marketing start

2009-09-01

Marketing end

0000-00-00

Substance

ACETAMINOPHEN;

Active strength

321 mg/1; mg/1; mg/

Pharmacologic classes

Central Nervous

DEA schedule

CIII

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record