NDC 71335-2581 – Azithromycin Dihydrate

Azithromycin Dihydrate 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2581

Product details

Brand name
Azithromycin Dihydrate
Generic name
Azithromycin dihydrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208249
Marketed since
February 15, 2024
Listing expires
December 31, 2027
Pharmacologic class
Macrolide Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Azithromycin Dihydrate →

Package NDC codes (5)

Package NDCDescriptionSince
71335-2581-130 TABLET, FILM COATED in 1 BOTTLE (71335-2581-1)Mar 13, 2025
71335-2581-25 TABLET, FILM COATED in 1 BOTTLE (71335-2581-2)Mar 13, 2025
71335-2581-32 TABLET, FILM COATED in 1 BOTTLE (71335-2581-3)Mar 13, 2025
71335-2581-46 TABLET, FILM COATED in 1 BOTTLE (71335-2581-4)Mar 13, 2025
71335-2581-54 TABLET, FILM COATED in 1 BOTTLE (71335-2581-5)Mar 13, 2025

Other Azithromycin Dihydrate products