Ketoprofen

Product NDC

63629-1836

11-digit product format

636291836

Labeler code

63629

Product ID

63629-1836_f0131449-7330-40f5-be8e-e536863c40e7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ketoprofen

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA073517

Marketing category

ANDA

Marketing start

1993-01-01

Marketing end

0000-00-00

Substance

KETOPROFEN

Active strength

75 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