CELEBREX

Product NDC

63629-6368

11-digit product format

636296368

Labeler code

63629

Product ID

63629-6368_f5de05ba-008f-4cdd-9f50-24dce418f08f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Celecoxib

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

NDA020998

Marketing category

NDA

Marketing start

1998-10-02

Marketing end

0000-00-00

Substance

CELECOXIB

Active strength

200 mg/1

Pharmacologic classes

Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record