NDC 50111-788 – Azithromycin

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

Human Prescription Drug

Product NDC50111-788

Product details

Brand name
Azithromycin
Generic name
Azithromycin
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065223
Marketed since
January 6, 2006
Listing expires
December 31, 2026
Pharmacologic class
Macrolide Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Azithromycin →

Package NDC codes (3)

Package NDCDescriptionSince
50111-788-1030 TABLET, FILM COATED in 1 BOTTLE (50111-788-10)Jan 6, 2006
50111-788-551 BLISTER PACK in 1 CARTON (50111-788-55) / 3 TABLET, FILM COATED in 1 BLISTER PACKFeb 18, 2014
50111-788-673 CARTON in 1 PACKAGE (50111-788-67) / 1 BLISTER PACK in 1 CARTON / 3 TABLET, FILM COATED in 1 BLISTER PACKJan 6, 2006

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