Zidovudine

Product NDC

57237-241

11-digit product format

572370241

Labeler code

57237

Product ID

57237-241_33d15753-c39d-4501-b724-7f30e7b299b6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Zidovudine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Citron Pharma LLC

Application

ANDA077267

Marketing category

ANDA

Marketing start

2005-09-19

Marketing end

0000-00-00

Substance

ZIDOVUDINE

Active strength

300 mg/1

Pharmacologic classes

Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record