Uses
Vasostrict ® is indicated to increase blood pressure in adults with vasodilatory shock who remain hypotensive despite fluids and catecholamines.
Source: US FDA prescribing information
Molecule
Vasopressin, unspecified is a prescription medicine indicated to increase blood pressure in adults with vasodilatory shock who remain hypotensive despite fluids and catecholamines. It is available as injection for intravenous use. MedsAcross supplies Vasopressin, unspecified for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.
Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review
From the regulator-approved product information. Each section names its source.
Vasostrict ® is indicated to increase blood pressure in adults with vasodilatory shock who remain hypotensive despite fluids and catecholamines.
Source: US FDA prescribing information
Vasopressin causes vasoconstriction by binding to V 1 receptors on vascular smooth muscle coupled to the Gq/11-phospholipase C-phosphatidyl-inositol-triphosphate pathway, resulting in the release of intracellular calcium. In addition, vasopressin stimulates antidiuresis via stimulation of V 2 receptors which are coupled to adenyl cyclase.
Source: US FDA prescribing information
Dilute 20 units/mL single dose vial or 200 units/10 mL (20 units/mL) multiple dose vial contents with normal saline (0.9% sodium chloride) or 5% dextrose in water (D5W) to either 0.1 units/mL or 1 unit/mL for intravenous administration. Discard unused diluted solution after 18 hours at room temperature or 24 hours under refrigeration. The 20 units/100 mL, 40 units/100 mL, 60 units/100 mL and 50 units/50 mL single dose vials do not require further dilution prior to administration. Post-cardiotomy shock: 0.03 to 0.1 units/minute. Septic shock: 0.01 to 0.07 units/minute
Source: US FDA prescribing information
Vasostrict ® 10 mL multiple dose vial is contraindicated in patients with known allergy or hypersensitivity to 8‑L-arginine vasopressin or chlorobutanol. The 1 mL single dose vial, 50 mL and 100 mL pre-mixed single dose vial does not contain chlorobutanol and is therefore contraindicated only in patients with a known allergy or hypersensitivity to 8-L-arginine vasopressin.
Source: US FDA prescribing information
Can worsen cardiac function. Reversible diabetes insipidus Worsening Cardiac Function A decrease in cardiac index may be observed with the use of vasopressin.
Source: US FDA prescribing information
The following adverse reactions associated with the use of vasopressin were identified in the literature. Because these reactions are reported voluntarily from a population of uncertain size, it is not possible to estimate their frequency reliably or to establish a causal relationship to drug exposure.
Source: US FDA prescribing information
Pressor effects of catecholamines and Vasostrict ® are expected to be additive. Indomethacin may prolong effects of Vasostrict ®. Co-administration of ganglionic blockers or drugs causing SIADH may increase the pressor response. Co-administration of drugs causing diabetes insipidus may decrease the pressor response.
Source: US FDA prescribing information
Store between 2°C and 8°C (36°F and 46°F). Do not freeze. Vials may be held up to 12 months upon removal from refrigeration to room temperature storage conditions (20°C to 25°C [68°F to 77°F], USP Controlled Room Temperature), anytime within the labeled shelf life. Once removed from refrigeration, unopened vial should be marked to indicate the revised 12 month expiration date. After initial entry into the 10 mL vial, the remaining contents must be refrigerated. Discard the refrigerated 10 mL vial after 30 days after first puncture.
Source: US FDA prescribing information
For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
4 presentations of Vasopressin, unspecified, sorted by availability.
| Medicine | Manufacturer | Register | Availability |
|---|---|---|---|
| Vasopressin, unspecified 20 units/mL injectionIntravenous Cold chainGeneric name | — | US FDA | Available on request |
| Vasostrict 20 units/mL injectionIntravenous Cold chain | Par Health | US FDA | Available on request |
| Vasostrict 0.2 units/mL injectionIntravenous Cold chain | Par Health | US FDA | Available on request |
| Vasostrict 0.4 units/mL injectionIntravenous Cold chain | Par Health | US FDA | Available on request |
1 brand names across 1 markets.
United States
Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.
| Register | Status | Source |
|---|---|---|
| US FDA | Not recorded | — |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US FDA (NDC directory, openFDA)Checked 12 November 2026 |
Yes, on request. MedsAcross lists 4 presentations of Vasopressin, unspecified and sources them for licensed hospitals, importers and physicians against valid import documents.
The catalogue lists 1 brand names for Vasopressin, unspecified, including Vasostrict.
At least one listed presentation of Vasopressin, unspecified must be kept cold, so it is shipped in temperature-controlled packaging. Check the storage line on each presentation.
Tell us the strength, quantity and destination country. Our team replies with availability, lead time and the import documents needed.