Ketoprofen

Product NDC

63629-3642

11-digit product format

636293642

Labeler code

63629

Product ID

63629-3642_d30a0ce3-e747-448a-98ab-6b5804003061

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ketoprofen

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

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

2019-12-31

Current FDA listing

Historical FDA.report record