Source: FDA, National Drug Code (US) Revision Year: 2021
DOPRAM Injection (doxapram hydrochloride injection, USP) is a clear, colorless, sterile, non-pyrogenic, aqueous solution with pH 3.5 to 5, for intravenous administration.
Each 1 mL contains:
Doxapram Hydrochloride, USP 20 mg
Benzyl Alcohol, NF (as preservative) 0.9%
Water for Injection, USP q.s.
Doxapram Injection is a respiratory stimulant.
Doxapram hydrochloride is a white to off-white, crystalline powder, sparingly soluble in water, alcohol and chloroform. Chemically, doxapram hydrochloride is 1-ethyl-4-[2-(4-morpholinyl)ethyl]-3,3-diphenyl-2-pyrrolidinone monohydrochloride, monohydrate.
The chemical structure is:
C24H31ClN2O2 • H2O M.W. 432.98
| How Supplied |
|---|
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DOPRAM Injection (doxapram hydrochloride injection, USP) is available in cartons of one 20 mL multiple dose vial containing 20 mg of doxapram hydrochloride per mL with benzyl alcohol 0.9% as the preservative (NDC 0641-6018-01). Manufactured by: Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ 07922 |
| Drug | Countries | |
|---|---|---|
| DOPRAM | France, Japan, Malta, Netherlands, Romania, United Kingdom, United States |
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