Deferoxamine mesylate

Product NDC

47781-623

11-digit product format

477810623

Labeler code

47781

Product ID

47781-623_1b81d47c-a02c-54f9-1bd0-290223496e26

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Deferoxamine mesylate

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS

Labeler

Alvogen Inc.

Application

ANDA207384

Marketing category

ANDA

Marketing start

2018-03-24

Marketing end

0000-00-00

Substance

DEFEROXAMINE MESYLATE

Active strength

500 mg/1

Pharmacologic classes

Iron Chelating Activity [MoA],Iron Chelator [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record