Ketorolac Tromethamine

Product NDC

21695-432

11-digit product format

216950432

Labeler code

21695

Product ID

21695-432_5914ef00-19b1-4e22-9ad3-2b62b455af9d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ketorolac Tromethamine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Rebel Distributors Corp

Application

ANDA074754

Marketing category

ANDA

Marketing start

2010-04-20

Marketing end

0000-00-00

Substance

KETOROLAC TROMETHAMINE

Active strength

10 mg/1

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record