Skip to main content

Alprostadil

NDC 71288-206 · Meitheal Pharmaceuticals Inc.

Generic nameAlprostadil
Dosage formINJECTION, SOLUTION, CONCENTRATE
RouteINTRAVASCULAR
Active ingredient(s)ALPROSTADIL
Strength500 ug/mL
Pharmacologic classGenitourinary Arterial Vasodilation [PE], Prostaglandin Analog [EPC], Prostaglandin E1 Agonist [EPC], Prostaglandin Receptor Agonists [MoA], Prostaglandins [CS], Venous Vasodilation [PE]
Marketing categoryANDA

Packages

71288-206-02 — 10 VIAL, SINGLE-USE in 1 CARTON (71288-206-02) / 1 mL in 1 VIAL, SINGLE-USE (71288-206-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0009-0215 — alprostadil, 0009-3169 — alprostadil, 0009-3701 — Alprostadil, 0009-5181 — Alprostadil, 0009-5182 — Alprostadil, 0009-7686 — Alprostadil, 52244-010 — alprostadil, 52244-020 — alprostadil, 52244-040 — alprostadil

Poisoning, adverse-effect and underdosing codes for this drug

The ICD-10-CM Table of Drugs and Chemicals carries these diagnosis codes for this drug — a drug-name match derived from FDA's product name and the Table of Drugs and Chemicals, not a CMS-published pairing.

T46.7X1 — Poisoning by peripheral vasodilators, accidental (unintentional), T46.7X2 — Poisoning by peripheral vasodilators, intentional self-harm, T46.7X3 — Poisoning by peripheral vasodilators, assault, T46.7X4 — Poisoning by peripheral vasodilators, undetermined, T46.7X5 — Adverse effect of peripheral vasodilators, T46.7X6 — Underdosing of peripheral vasodilators

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