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azithromycin dihydrate

NDC 70436-222 · Slate Run Pharmaceuticals, LLC

Generic nameazithromycin dihydrate
Dosage formPOWDER, FOR SUSPENSION
RouteORAL
Active ingredient(s)AZITHROMYCIN DIHYDRATE
Strength200 mg/5mL
Pharmacologic classMacrolide Antimicrobial [EPC], Macrolides [CS]
Marketing categoryANDA

Packages

70436-222-36 — 1 BOTTLE in 1 CARTON (70436-222-36) / 30 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8702 — Azithromycin, 68788-8773 — Azithromycin dihydrate, 68788-8800 — Azithromycin Dihydrate, 69306-250 — Azithromycin, 69452-171 — Azithromycin, 69452-172 — Azithromycin, 69452-173 — Azithromycin, 70436-019 — Azithromycin Dihydrate, 70436-220 — azithromycin dihydrate, 70436-221 — azithromycin dihydrate, 70436-228 — azithromycin dihydrate, 70518-2433 — Azithromycin, 70518-3168 — Azithromycin Dihydrate, 70518-3254 — Azithromycin, 70518-4105 — Azithromycin dihydrate, 70518-4160 — Azithromycin Dihydrate, 70518-4202 — Azithromycin dihydrate, 70518-4356 — azithromycin, 70518-4367 — azithromycin, 70710-1457 — 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.