Azithromycin

Product NDC

63739-575

11-digit product format

637390575

Labeler code

63739

Product ID

63739-575_1998db12-6000-44a9-ad8a-2ffea3edfb8d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Azithromycin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA065211

Marketing category

ANDA

Marketing start

2013-12-02

Marketing end

0000-00-00

Substance

AZITHROMYCIN MONOHYDRATE

Active strength

250 mg/1

Pharmacologic classes

Macrolide Antimicrobial [EPC],Macrolides [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record