Azithromycin

Product NDC

70518-0712

11-digit product format

705180712

Labeler code

70518

Product ID

70518-0712_a565c33a-e8d6-548e-e053-2995a90a7146

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Azithromycin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA065211

Marketing category

ANDA

Marketing start

2017-08-25

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

2021-12-31

Current FDA listing

Historical FDA.report record