Azacitidine

Product NDC

16714-777

11-digit product format

167140777

Labeler code

16714

Product ID

16714-777_40820b04-64ba-4fee-9b70-dcc8a027eae3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Azacitidine

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS; SUBCUTANEOUS

Labeler

NorthStar RxLLC

Application

ANDA209540

Marketing category

ANDA

Marketing start

2018-05-04

Marketing end

0000-00-00

Substance

AZACITIDINE

Active strength

100 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record