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Azithromycin Dihydrate

NDC 83112-501 · Health Department, Oklahoma State

Generic nameAzithromycin Dihydrate
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)AZITHROMYCIN DIHYDRATE
Strength500 mg/1
Pharmacologic classMacrolide Antimicrobial [EPC], Macrolides [CS]
Marketing categoryANDA

Packages

83112-501-00 — 2 TABLET, FILM COATED in 1 PACKET (83112-501-00)

83112-501-02 — 2 TABLET, FILM COATED in 1 PACKET (83112-501-02)

83112-501-04 — 4 TABLET, FILM COATED in 1 PACKET (83112-501-04)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72673-081 — Azithromycin, 72673-082 — Azithromycin, 72673-083 — Azithromycin, 72673-084 — Azithromycin, 72789-081 — Azithromycin Dihydrate, 72789-445 — Azithromycin dihydrate, 72789-483 — Azithromycin Dihydrate, 76420-046 — Azithromycin Dihydrate, 76420-213 — Azithromycin, 76420-649 — Azithromycin, 80425-0218 — Azithromycin Dihydrate, 80425-0220 — Azithromycin Dihydrate, 80425-0412 — azithromycin dihydrate, 80425-0431 — azithromycin dihydrate, 82804-153 — Azithromycin dihydrate, 82804-182 — Azithromycin Dihydrate, 82804-214 — azithromycin, 83008-081 — Azithromycin Dihydrate, 85766-008 — Azithromycin, 85766-042 — Azithromycin dihydrate, +134 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.