FDA LABEL RECORD
Vasopressin in 0.9% Sodium Chloride
VASOPRESSIN. FDA prescribing information for this product, as published on the retrieval date below.
AS THE LABEL RECORDS IT
Product details
| Brand name | Vasopressin in 0.9% Sodium Chloride |
|---|---|
| Generic name | VASOPRESSIN |
| Labeller | Long Grove Pharmaceuticals, LLC |
| Route | INTRAVENOUS |
| Label version | 10 |
| Effective | 2025-06-17 |
| Retrieved by this site | 2026-10-03 |
| Full label | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=bf4b0b63-0055-40d8-b331-7f9f1ea3214c |
INDICATIONS AND USAGE
Quoted from the FDA label
1 INDICATIONS AND USAGE Vasopressin in Sodium Chloride Injection is indicated to increase blood pressure in adults with vasodilatory shock who remain hypotensive despite fluids and catecholamines. Vasopressin in Sodium Chloride Injection is indicated to increase blood pressure in adults with vasodilatory shock who remain hypotensive despite fluids and catecholamines. ( 1 )
What this page is
A reproduction of a public FDA label record. Everything quoted above is the labeller's wording as published by the FDA, not this site's. Nothing here is regulatory, legal or medical advice, and a label being reproduced says nothing about whether a product is available in any particular country. Labels are revised often; the retrieval date above says when this copy was taken, and the full current label is at the link.
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