Skip to main content

EPHEDRINE SULFATE

NDC 42023-243 · Par Health USA, LLC

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameEphedrine Sulfate
Dosage formINJECTION
RouteINTRAVENOUS
Active ingredient(s)EPHEDRINE SULFATE
Strength5 mg/mL
Pharmacologic classAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Increased Norepinephrine Activity [PE], Norepinephrine Releasing Agent [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
Marketing categoryNDA

Packages

42023-243-01 — 10 mL in 1 VIAL, SINGLE-DOSE (42023-243-01)

42023-243-99 — 10 mL in 1 VIAL, SINGLE-DOSE (42023-243-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0641-6236 — Ephedrine Sulfate, 0641-6238 — Ephedrine Sulfate, 0781-3269 — Ephedrine Sulfate, 14789-250 — Ephedrine Sulfate, 14789-251 — Ephedrine Sulfate, 14789-252 — Ephedrine Sulfate, 16714-037 — Ephedrine Sulfate, 25021-836 — Ephedrine Sulfate, 36000-336 — ephedrine sulfate, 42023-216 — Ephedrine Sulfate, 43598-725 — Ephedrine sulfate, 51662-1325 — EPHEDRINE SULFATE, 51754-4200 — ephedrine sulfate, 51754-4250 — ephedrine sulfate, 55150-373 — Ephedrine Sulfate, 65145-158 — Ephedrine Sulfate, 65219-257 — Ephedrine Sulfate, 65219-546 — ephedrine sulfate, 65219-548 — ephedrine sulfate, 68083-495 — Ephedrine Sulfate, +18 more

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