Decitabine

Product NDC

0781-3139

11-digit product format

007813139

Labeler code

0781

Product ID

0781-3139_0b9599e8-9018-42ee-b247-e2a944c36510

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Decitabine

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Sandoz Inc

Application

ANDA202969

Marketing category

ANDA

Marketing start

2014-08-28

Marketing end

0000-00-00

Substance

DECITABINE

Active strength

50 mg/50mL

Pharmacologic classes

Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record