Celecoxib

Product NDC

71335-0361

11-digit product format

713350361

Labeler code

71335

Product ID

71335-0361_b9555f14-a37f-42bb-ad52-95f9192c09c0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Celecoxib

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA204197

Marketing category

ANDA

Marketing start

2015-06-03

Marketing end

0000-00-00

Substance

CELECOXIB

Active strength

200 mg/1

Pharmacologic classes

Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record