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Azithromycin Dihydrate

NDC 68071-3661 · NuCare Pharmaceuticals,Inc.

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

68071-3661-2 — 2 TABLET, FILM COATED in 1 BOTTLE (68071-3661-2)

68071-3661-5 — 5 TABLET, FILM COATED in 1 BOTTLE (68071-3661-5)

68071-3661-6 — 6 TABLET, FILM COATED in 1 BOTTLE (68071-3661-6)

68071-3661-7 — 7 TABLET, FILM COATED in 1 BOTTLE (68071-3661-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-1502 — Azithromycin Dihydrate, 67046-1503 — azithromycin dihydrate, 67046-1607 — Azithromycin dihydrate, 67296-0020 — azithromycin dihydrate, 67296-1942 — Azithromycin dihydrate, 67296-1945 — Azithromycin, 67296-2141 — Azithromycin, 67296-2185 — Azithromycin Dihydrate, 68071-2266 — Azithromycin, 68071-2297 — Azithromycin, 68071-3715 — Azithromycin Dihydrate, 68071-4779 — Azithromycin, 68071-4812 — Azithromycin, 68071-4902 — Azithromycin, 68071-4976 — Azithromycin, 68071-5058 — Azithromycin, 68071-5082 — Azithromycin, 68094-690 — Azithromycin dihydrate, 68094-799 — Azithromycin dihydrate, 68094-900 — 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.