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PAPAVERINE INJECTION 6MG/2ML 10X2ML - 30 mg/mL INJECTION, SOLUTION
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PAPAVERINE INJECTION 6MG/2ML 10X2ML

Generic: Papaverine Hydrochloride

PAPAVERINE INJECTION 6MG/2ML 10X2ML

NDC:54288-0142-10
Manufacturer:BPI Labs LLC
Strength:30 mg/mL
Dosage Form:INJECTION, SOLUTION
Route:INTRAMUSCULAR, INTRAVENOUS, PARENTERAL

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Drug Information

Identification

Generic Name

Papaverine Hydrochloride

Brand Name

PAPAVERINE HYDROCHLORIDE

Labeler / Distributor

BPI Labs LLC

Product Type

HUMAN PRESCRIPTION DRUG

Administration

Dosage Form

INJECTION, SOLUTION

Route of Administration

INTRAMUSCULAR, INTRAVENOUS, PARENTERAL

Active Ingredients

IngredientStrength
PAPAVERINE HYDROCHLORIDE30 mg/mL

Data sourced from openFDA / DailyMed. For full prescribing information, consult the drug label.

Clinical Drug Information

Indications & Usage

INDICATIONS AND USAGE Papaverine is recommended in various conditions accompanied by spasm of smooth muscle, such as vascular spasm associated with acute myocardial infarction (coronary occlusion), angina pectoris, peripheral and pulmonary embolism, peripheral vascular disease in which there is a vasospastic element, or certain cerebral angiospastic states, and visceral spasm , as in ureteral, biliary, or gastrointestinal colic.

Dosage & Administration

DOSAGE AND ADMINISTRATION Papaverine Hydrochloride may be administered intravenously or intramuscularly. The intravenous route is recommended when an immediate effect is desired, but the drug must be injected slowly over the course of 1 or 2 minutes to avoid uncomfortable or alarming side effects. Parenteral administration of papaverine hydrochloride in doses of 1 to 4 mL is repeated every 3 hours as indicated. In the treatment of cardiac extrasystoles, 2 doses may be given 10 minutes apart.

Adverse Reactions

ADVERSE REACTIONS The following side effects have been reported: general discomfort, nausea, abdominal discomfort, anorexia, constipation or diarrhea, skin rash, malaise, vertigo, headache, intensive flushing of the face, perspiration, increase in the depth of respiration, increase in heart rate, a slight rise in blood pressure, and excessive sedation. Hepatitis, probably related to an immune mechanism, has been reported infrequently. Rarely, this has progressed to cirrhosis. To report SUSPECTED ADVERSE REACTIONS, contact BPI Labs, LLC at (727) 471-0850 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

Clinical data sourced from openFDA drug labeling. For complete prescribing information, consult the full drug label.