Dexamethasone

NDC 70771-1707 · Zydus Lifesciences Limited

Generic nameDexamethasone

Dosage formTABLET

RouteORAL

Active ingredient(s)DEXAMETHASONE

Strength1.5 mg/1

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

Marketing categoryANDA

Packages

70771-1707-1 — 100 TABLET in 1 BOTTLE (70771-1707-1)

FDA lists these products with the same active ingredient.

70518-1534 — Dexamethasone, 70518-3994 — Tobramycin and Dexamethasone, 70518-4320 — Dexamethasone, 70518-4669 — Dexamethasone, 70771-1699 — Dexamethasone, 70771-1700 — Dexamethasone, 70771-1701 — Dexamethasone, 70771-1704 — Dexamethasone, 70771-1705 — Dexamethasone, 70771-1706 — Dexamethasone, 70954-398 — Dexamethasone, 70954-399 — Dexamethasone, 70954-401 — Dexamethasone, 70954-402 — Dexamethasone, 70954-403 — Dexamethasone, 70954-404 — Dexamethasone, 70954-872 — Dexamethasone, 71205-012 — DEXAMETHASONE, 71205-013 — DEXAMETHASONE, 71205-330 — Neomycin and Polymyxin B Sulfates and 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.