EPINEPHRINE

NDC 51662-1321 · HF Acquisition Co LLC, DBA HealthFirst

Generic nameEPINEPHRINE

Dosage formINJECTION, SOLUTION

RouteINTRAMUSCULAR

Active ingredient(s)EPINEPHRINE

Strength.15 mg/.15mL

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

Marketing categoryNDA

Packages

51662-1321-1 — .15 mL in 1 DOSE PACK (51662-1321-1)

51662-1321-2 — 2 DOSE PACK in 1 CARTON (51662-1321-2) / .15 mL in 1 DOSE PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-5254 — Epinephrine, 50090-7037 — Epinephrine, 51662-1222 — EPINEPHRINE, 51662-1223 — EPINEPHRINE, 51662-1224 — EPINEPHRINE, 51662-1225 — EPINEPHRINE, 51662-1232 — LIDOCAINE HCI, 51662-1290 — ADRENALIN (EPINEPHRINE), 51662-1307 — ADRENALIN(R), 51662-1320 — EPINEPHRINE, 51662-1395 — LIDOCAINE HCI AND EPINEPHRINE, 51662-1419 — LIDOCAINE HCI, 51662-1476 — EPINEPHRINE, 51662-1503 — LIDOCAINE HCl AND EPINEPHRINE, 51662-1504 — LIDOCAINE HCl AND EPINEPHRINE, 51662-1531 — EPINEPHRINE, 51662-1629 — EPINEPHRINE, 51662-1661 — AUVI-Q, 51662-1662 — AUVI-Q, 51662-1663 — AUVI-Q, +245 more

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