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Droxidopa

NDC 70710-1391 · Zydus Pharmaceuticals USA Inc.

Generic nameDroxidopa
Dosage formCAPSULE
RouteORAL
Active ingredient(s)DROXIDOPA
Strength300 mg/1
Pharmacologic classCatecholamines [CS], Increased Blood Pressure [PE]
Marketing categoryANDA

Packages

70710-1391-9 — 90 CAPSULE in 1 BOTTLE (70710-1391-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68180-987 — DROXIDOPA, 68180-988 — DROXIDOPA, 68180-989 — DROXIDOPA, 69452-256 — DROXIDOPA, 69452-257 — DROXIDOPA, 69452-258 — DROXIDOPA, 70436-140 — droxidopa, 70436-141 — droxidopa, 70436-142 — droxidopa, 70710-1389 — Droxidopa, 70710-1390 — Droxidopa, 70771-1609 — Droxidopa, 70771-1610 — Droxidopa, 70771-1611 — Droxidopa, 72205-072 — Droxidopa, 72205-073 — Droxidopa, 72205-074 — Droxidopa, 82249-551 — Droxidopa, 82249-552 — Droxidopa, 82249-554 — Droxidopa, +24 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels