Epinephrine

Product NDC
50090-5254
11-digit product format
500905254
Labeler code
50090
Product ID
50090-5254_42449017-67a2-4443-b5de-dbdce65bc95e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Epinephrine
Dosage form
INJECTION
Route
INTRAMUSCULAR; SUBCUTANEOUS
Labeler
A-S Medication Solutions
Application
ANDA090589
Marketing category
ANDA
Marketing start
2019-08-19
Substance
EPINEPHRINE
Active strength
.15 mg/.3mL
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
50090-5254-0500905254002 CONTAINER in 1 CARTON (50090-5254-0) / 1 mL in 1 CONTAINER2 container2020-10-14NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
EpinephrineA-S Medication Solutions2025-11-10HUMAN PRESCRIPTION DRUG LABEL10
EpinephrineA-S Medication Solutions2023-12-16HUMAN PRESCRIPTION DRUG LABEL8