Azithromycin

Product NDC

70518-2075

11-digit product format

705182075

Labeler code

70518

Product ID

70518-2075_88dfaa6f-474c-f8a9-e053-2995a90a646a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Azithromycin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA211147

Marketing category

ANDA

Marketing start

2019-05-13

Marketing end

0000-00-00

Substance

AZITHROMYCIN DIHYDRATE

Active strength

200 mg/5mL

Pharmacologic classes

Macrolide Antimicrobial [EPC],Macrolides [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record