FDA LABEL RECORD
ANGIOTENSIN II
ANGIOTENSIN II. FDA prescribing information for this product, as published on the retrieval date below.
AS THE LABEL RECORDS IT
Product details
| Brand name | ANGIOTENSIN II |
|---|---|
| Generic name | ANGIOTENSIN II |
| Labeller | Gland Pharma Limited |
| Route | INTRAVENOUS |
| Label version | 3 |
| Effective | 2025-06-04 |
| Retrieved by this site | 2026-10-03 |
| Full label | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=727d1102-fc46-46f8-b78e-fd13f0738fe4 |
INDICATIONS AND USAGE
Quoted from the FDA label
1 INDICATIONS AND USAGE Angiotensin II Injection increases blood pressure in adults with septic or other distributive shock. Angiotensin II Injection is a vasoconstrictor to increase blood pressure in adults with septic or other distributive shock. (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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