Ketoprofen

Product NDC

43063-737

11-digit product format

430630737

Labeler code

43063

Product ID

43063-737_7fc14419-dc27-80b4-e053-2991aa0a1a43

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ketoprofen

Dosage form

CAPSULE

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA073516

Marketing category

ANDA

Marketing start

1993-01-01

Marketing end

0000-00-00

Substance

KETOPROFEN

Active strength

50 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

2020-12-31

Current FDA listing

Historical FDA.report record