Fenoprofen Calcium

Product NDC

55289-334

11-digit product format

552890334

Labeler code

55289

Product ID

55289-334_7c1ef4c9-4b19-6d43-e053-2991aa0ac908

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fenoprofen Calcium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA072267

Marketing category

ANDA

Marketing start

2012-11-14

Marketing end

0000-00-00

Substance

FENOPROFEN CALCIUM

Active strength

600 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