EPINEPHRINE
EPINEPHRINE INJ. USP, 0.1 mg/mL 1mg per 10mL LUER-JET™ SYR
Approved
Approval ID
e651aebd-f619-c3a6-e053-2995a90aea01
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 15, 2022
Manufacturers
FDA
HF Acquisition Co LLC, DBA HealthFirst
DUNS: 045657305
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
EPINEPHRINE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51662-1381
Product Classification
G
Generic Name
EPINEPHRINE
Product Specifications
Route of AdministrationINTRACARDIAC, INTRAVENOUS
Effective DateAugust 15, 2022
FDA Product Classification
INGREDIENTS (6)
SODIUM BISULFITEInactive
Code: TZX5469Z6I
Classification: IACT
SODIUM CITRATEInactive
Code: 1Q73Q2JULR
Classification: IACT
CITRIC ACID MONOHYDRATEInactive
Code: 2968PHW8QP
Classification: IACT
EPINEPHRINEActive
Quantity: 0.1 mg in 1 mL
Code: YKH834O4BH
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT