EPINEPHRINE

NDC 70518-4156 · REMEDYREPACK INC.

Generic nameEPINEPHRINE

Dosage formINJECTION

RouteINTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

Active ingredient(s)EPINEPHRINE

Strength1 mg/mL

Pharmacologic classAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Catecholamine [EPC], Catecholamines [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]

Marketing categoryNDA

Packages

70518-4156-0 — 25 VIAL in 1 CARTON (70518-4156-0) / 1 mL in 1 VIAL (70518-4156-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70163-0035 — Adrenalinum, Ragweed, Pollen (Ambrosia Artemisiaefolia), Apis Mellifica, Echinacea (Angustifolia), Histaminum Hydrochloricum, Ledum Palustre, Lycopodium Clavatum, Natrum Muriaticum, Sulphur, 70385-2019 — Epinephrine 0.3 Adults, 70385-2020 — Epinephrine 0.15 Pediatrics, 70385-2022 — Epinephrine 0.3 Adults, 70385-2024 — epinephrine, 70385-2038 — Epinephrine 0.15 Pediatrics, 70518-1342 — epinephrine, 70518-2048 — epinephrine, 70518-2283 — Epinephrine, 70518-3816 — Epinephrine, 70518-4274 — EPINEPHRINE, 70518-4573 — epinephrine, 71872-7117 — Epinephrine, 71872-7134 — Epinephrine, 71872-7135 — Epinephrine, 71872-7172 — epinephrine, 71872-7173 — epinephrine, 71872-7223 — epinephrine, 71872-7250 — epinephrine, 71872-7304 — Epinephrine, +245 more

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