Skip to main content

droxidopa

NDC 63304-086 · Sun Pharmaceutical Industries, Inc.

Generic namedroxidopa

Dosage formCAPSULE

RouteORAL

Active ingredient(s)DROXIDOPA

Strength100 ug/1

Pharmacologic classCatecholamines [CS], Increased Blood Pressure [PE]

Marketing categoryANDA

Packages

63304-086-90 — 90 CAPSULE in 1 BOTTLE (63304-086-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

31722-015 — Droxidopa, 50228-429 — droxidopa, 50228-430 — droxidopa, 50228-431 — droxidopa, 51407-765 — droxidopa, 51407-766 — droxidopa, 51407-767 — droxidopa, 59651-375 — Droxidopa, 59651-376 — Droxidopa, 59651-377 — Droxidopa, 63304-104 — droxidopa, 63304-112 — droxidopa, 67386-820 — droxidopa, 67386-821 — droxidopa, 67386-822 — droxidopa, 67877-704 — Droxidopa, 67877-705 — Droxidopa, 67877-706 — Droxidopa, 68180-987 — DROXIDOPA, 68180-988 — 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