Azithromycin Dihydrate

NDC 71205-491 · Proficient Rx LP

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

71205-491-03 — 3 TABLET, FILM COATED in 1 BLISTER PACK (71205-491-03)

71205-491-04 — 4 TABLET, FILM COATED in 1 BLISTER PACK (71205-491-04)

FDA lists these products with the same active ingredient.

70771-1422 — Azithromycin, 70771-1423 — Azithromycin, 70771-1424 — Azithromycin, 70771-1425 — Azithromycin, 71093-174 — Azithromycin Dihydrate, 71093-175 — Azithromycin Dihydrate, 71205-158 — Azithromycin, 71205-216 — Azithromycin, 71205-424 — Azithromycin, 71205-430 — Azithromycin Dihydrate, 71205-503 — Azithromycin, 71205-519 — Azithromycin, 71205-645 — Azithromycin, 71205-674 — Azithromycin, 71335-1755 — Azithromycin, 71335-2581 — Azithromycin dihydrate, 72162-2668 — Azithromycin, 72162-2669 — Azithromycin, 72189-015 — AZITHROMYCIN, 72189-087 — AZITHROMYCIN, +134 more

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