FENOPROFEN CALCIUM

Product NDC

54288-131

11-digit product format

542880131

Labeler code

54288

Product ID

54288-131_a03faba1-e4b5-4c21-988a-64dbcf0d6a61

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

FENOPROFEN CALCIUM

Dosage form

CAPSULE

Route

ORAL

Labeler

BPI Labs LLC

Application

NDA017604

Marketing category

NDA

Marketing start

2016-07-06

Marketing end

0000-00-00

Substance

FENOPROFEN CALCIUM

Active strength

200 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

2017-12-31

Current FDA listing

Historical FDA.report record