Azithromycin

Product NDC

25021-112

11-digit product format

250210112

Labeler code

25021

Product ID

25021-112_4f18e9b5-3244-42b3-92a6-c0dc46e69076

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

azithromycin

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Sagent Pharmaceuticals

Application

ANDA065506

Marketing category

ANDA

Marketing start

2009-05-01

Marketing end

2019-12-01

Substance

AZITHROMYCIN MONOHYDRATE

Active strength

500 mg/5mL

Pharmacologic classes

Macrolide Antimicrobial [EPC],Macrolides [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record