Epinephrine

Product NDC
50090-7037
11-digit product format
500907037
Labeler code
50090
Product ID
50090-7037_71f5111d-2a54-4b3e-a7d8-eb20f504b341
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Epinephrine
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
A-S Medication Solutions
Application
NDA211363
Marketing category
NDA
Marketing start
2023-01-30
Substance
EPINEPHRINE
Active strength
.1 mg/mL
Pharmacologic classes
Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Catecholamine [EPC], Catecholamines [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
YKH834O4BHEPINEPHRINE51-43-4EPINEPHRINE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
50090-7037-0500907037001 CARTON in 1 PACKAGE (50090-7037-0) / 1 mL in 1 CARTON1 carton2024-01-10NoNoHistorical
50090-7037-15009070370110 CARTON in 1 PACKAGE (50090-7037-1) / 1 mL in 1 CARTON10 carton2024-01-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
EpinephrineA-S Medication Solutions2024-01-15HUMAN PRESCRIPTION DRUG LABEL4