Celecoxib

Product NDC

68071-2169

11-digit product format

680712169

Labeler code

68071

Product ID

68071-2169_46f1e0ac-d67c-4419-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Celecoxib

Dosage form

CAPSULE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA204197

Marketing category

ANDA

Marketing start

2015-06-03

Marketing end

0000-00-00

Substance

CELECOXIB

Active strength

100 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record