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No-SPA injection (drotaverine hydrochloride) is a potent antispasmodic (smooth muscle relaxant) used to relieve spasms in organs like the gastrointestinal tract, biliary tract, and urinary system. The injectable form enables rapid action in acute colicky pain, muscle spasm, or smooth-muscle disorders.
Active ingredient: Drotaverine hydrochloride — 40 mg per 2 ml ampoule
Excipients / inactives: May include sodium metabisulfite, ethanol, water for injection, buffer salts (depending on manufacturer)
Antispasmodic / Myotropic Smooth Muscle Relaxant
Sterile injectable solution in ampoule — 2 ml per ampoule containing 40 mg drotaverine.
No-SPA injection is indicated for:
Relief of smooth muscle spasm (colic pain) in biliary tract (gallbladder, bile ducts)
Ureteric colic, renal colic (urinary tract spasm)
Gastrointestinal smooth muscle spasms (intestinal, pyloric, enteric colic)
Gynecological spasm (e.g., dysmenorrhea, uterine spasm) in some settings
For adults, typical doses range from one ampoule (40 mg / 2 ml) by intramuscular (IM) or slow intravenous (IV) injection, depending on severity.
In acute colic, 1 or 2 ampoules may be given via slow IV injection (in some protocols)
Doses may be repeated depending on response and physician direction, but not exceeding safe limits (e.g. 1-3 injections daily)
Pediatric use: Safety and dosage in children are less well established; only under specialist supervision.
Overdose may lead to hypotension, cardiac arrhythmias, bradycardia, respiratory depression, or circulatory collapse.
Management: supportive care, cardiovascular monitoring, intravenous fluids, symptomatic and intensive care as needed.
There is no specific antidote; treatment is supportive.
Typically, as injectable medication is administered by healthcare providers, “missed dose” is less relevant.
Follow the prescribing physician’s plan; do not self-administer or double dose.
Administer intramuscular (IM) or **slow intravenous (IV) injection.
IV administration should be done slowly to avoid sudden vasodilation or hypotension.
Use aseptic technique; ensure correct dilution (if required) and monitoring during and after injection.
Monitor vital signs, especially blood pressure and cardiac rhythm.
Known hypersensitivity to drotaverine or any component of the formulation (e.g. metabisulfite)
Severe hepatic or renal impairment (use with caution)
Pregnancy and breastfeeding: only if benefit outweighs risk (consult specialist)
Patients with known sulfite sensitivity (some formulations contain sodium metabisulfite)
Caution or avoid in conditions where vasodilation or drop in blood pressure can be dangerous
Common / Less serious:
Hypotension, palpitation
Local reactions at injection site (pain, redness, swelling)
Nausea, gastrointestinal discomfort
Rare / Serious:
Allergic reactions (rash, itching, swelling, anaphylaxis)
Severe hypotension, syncope
Cardiac arrhythmias in predisposed patients
Respiratory depression in overdose cases
Monitor blood pressure and cardiovascular status in at-risk patients
Use with caution in patients with liver or kidney disease
Avoid co-administration with other vasodilators without careful monitoring
May impair ability to perform tasks requiring alertness (e.g. driving) if side effects occur
Inform healthcare providers about therapy before surgical/dental procedures
In formulations containing sulfites, caution in patients with asthma or sulfite sensitivity
Risk of additive hypotensive effect with other vasodilators or antihypertensives
Drugs that affect cardiac conduction or rhythm may interact in susceptible patients
Other smooth muscle relaxants may potentiate effects
Because drotaverine acts via phosphodiesterase inhibition, caution with other PDE inhibitors (though specific interactions are less well documented)
Store below 30 °C in a dry place, protected from light.
Do not freeze
Use before expiry date
Dispose unused or expired ampoules per medical / pharmaceutical waste regulation
Not a narcotic or controlled substance, but prescription-only and must be administered under medical supervision
Administer slowly by IV when needed, especially in colic pain
Monitor blood pressure before and after administration
Avoid combining with other potent vasodilators without supervision
Be cautious in patients with cardiovascular disease
In patients with sulfite sensitivity, check formulation ingredients
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