APPLICATION
NDA205029
TYPE
NDA
ORIGINAL APPROVAL
2014-07-29
LATEST ACTION
2025-06-30
ROUTE
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS, INTRAOCULAR, INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS, INTRAVENOUS, INTRAOCULAR, INTRAMUSCULAR, SUBCUTANEOUS
DOSAGE FORM
SOLUTION
MARKETING STATUS
Prescription, Discontinued
Products
EPINEPHRINE · ReferencePrescription
EPINEPHRINE 30MG/30ML (1MG/ML) · SOLUTION · INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
EPINEPHRINE · ReferencePrescription
EPINEPHRINE 10MG/10ML (1MG/ML) · SOLUTION · INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
EPINEPHRINE · ReferencePrescription
EPINEPHRINE 1MG/ML (1MG/ML) · SOLUTION · INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
EPINEPHRINE · ReferenceDiscontinued
EPINEPHRINE 1MG/ML (1MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SOLUTION · INTRAVENOUS
EPINEPHRINE · ReferencePrescription
EPINEPHRINE 1MG/ML (1MG/ML) · SOLUTION · INTRAVENOUS, INTRAOCULAR, INTRAMUSCULAR, SUBCUTANEOUS
Approval history
2015-12-03Manufacturing (CMC) · Supplement 3 · standardAP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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