azithromycin

Product NDC

10019-648

11-digit product format

100190648

Labeler code

10019

Product ID

10019-648_c9cf5e72-5b34-4ed4-9fe0-fda76921fd89

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

azithromycin

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Baxter Healthcare Corporation

Application

NDA050733

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

1997-01-01

Marketing end

0000-00-00

Substance

AZITHROMYCIN DIHYDRATE

Active strength

100 mg/mL

Pharmacologic classes

Macrolide Antimicrobial [EPC],Macrolides [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record