DOXAPRAM HYDROCHLORIDE
DOPRAM INJECTION (DOXAPRAM HYDROCHLORIDE INJECTION, USP) 400 mg/20 mL (20 mg/mL) 20 mL VIAL BOXED
Approved
Approval ID
954859c0-a121-34d6-e053-2a95a90a1e19
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 22, 2020
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.
DOXAPRAM HYDROCHLORIDE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51662-1404
Application NumberNDA014879
Product Classification
M
Marketing Category
C73594
G
Generic Name
DOXAPRAM HYDROCHLORIDE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateFebruary 22, 2020
FDA Product Classification
INGREDIENTS (3)
BENZYL ALCOHOLInactive
Quantity: 9 mg in 1 mL
Code: LKG8494WBH
Classification: IACT
DOXAPRAM HYDROCHLORIDEActive
Quantity: 20 mg in 1 mL
Code: P5RU6UOQ5Y
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT