Dexamethasone

NDC 70771-1701 · Zydus Lifesciences Limited

Generic nameDexamethasone

Dosage formTABLET

RouteORAL

Active ingredient(s)DEXAMETHASONE

Strength2 mg/1

Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

Marketing categoryANDA

Packages

70771-1701-1 — 100 TABLET in 1 BOTTLE (70771-1701-1)

FDA lists these products with the same active ingredient.

69452-278 — Dexamethasone, 69918-515 — neomycin sulfate, polymyxin b sulfate and dexamethasone, 70244-033 — Ciprofloxacin and dexamethasone, 70382-204 — dexamethasone, 70518-1534 — Dexamethasone, 70518-3994 — Tobramycin and Dexamethasone, 70518-4320 — Dexamethasone, 70518-4669 — Dexamethasone, 70771-1699 — Dexamethasone, 70771-1700 — Dexamethasone, 70771-1704 — Dexamethasone, 70771-1705 — Dexamethasone, 70771-1706 — Dexamethasone, 70771-1707 — Dexamethasone, 70954-398 — Dexamethasone, 70954-399 — Dexamethasone, 70954-401 — Dexamethasone, 70954-402 — Dexamethasone, 70954-403 — Dexamethasone, 70954-404 — Dexamethasone, +187 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.