Romidepsin

Product NDC

0703-3071

11-digit product format

007033071

Labeler code

0703

Product ID

0703-3071_1c266507-2ce7-4531-9f05-b3e7820b0fea

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Romidepsin

Dosage form

INJECTION, SOLUTION, CONCENTRATE

Route

INTRAVENOUS

Labeler

Teva Parenteral Medicines, Inc.

Application

NDA208574

Marketing category

NDA

Marketing start

2020-04-14

Marketing end

0000-00-00

Substance

ROMIDEPSIN

Active strength

5 mg/mL

Pharmacologic classes

Histone Deacetylase Inhibitor [EPC],Histone Deacetylase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record