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EPHEDRINE SULFATE

NDC 70069-819 · Somerset Therapeutics, LLC

Generic nameEPHEDRINE SULFATE
Dosage formINJECTION
RouteINTRAVENOUS
Active ingredient(s)EPHEDRINE SULFATE
Strength50 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 categoryANDA

Packages

70069-819-10 — 10 VIAL in 1 CARTON (70069-819-10) / 1 mL in 1 VIAL

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68083-610 — Ephedrine Sulfate, 69536-250 — EPHEDRINE SULFATE, 69842-922 — Ephedrine Sulfate, 70121-1637 — Ephedrine Sulfate, 70518-4433 — EPHEDRINE SULFATE, 70700-249 — Ephedrine Sulfate, 70756-611 — Ephedrine sulfate, 71872-7257 — Ephedrine Sulfate, 71872-7269 — Ephedrine Sulfate, 71872-7276 — Ephedrine Sulfate, 71872-7302 — Ephedrine sulfate, 71872-7336 — Ephedrine Sulfate, 71872-7378 — 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.