Quick answers
- What is Desmopressin acetate used for?
- The FDA-approved label (Ddavp, Ferring Pharmaceuticals Inc., September 28, 2022) says: “DDAVP Injection is a vasopressin analog used for: Central Diabetes Insipidus - as antidiuretic replacement therapy in the management of central (cranial) diabetes insipidus and for the management of the temporary polyuria and polydipsia following head trauma or surgery in the pituitary region. …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Desmopressin acetate have a boxed warning?
- Yes. The FDA label for Ddavp has a boxed warning, the FDA’s strongest warning. Read it on the full label and ask your pharmacist.
- Is there a shortage of Desmopressin acetate?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Desmopressin acetate been recalled?
- FDA enforcement reports list 1 recall of products of this medicine; the newest started November 23, 2022 (Class II). A recall usually concerns specific lots, not every product.
- Who makes Desmopressin acetate?
- 27 companies list prescription products of Desmopressin acetate in the FDA NDC Directory, including Nordic Pharma, Inc., Ferring Pharmaceuticals Inc. and Sun Pharmaceutical Industries, Inc..
What Desmopressin acetate is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
DDAVP Injection is a vasopressin analog used for: Central Diabetes Insipidus - as antidiuretic replacement therapy in the management of central (cranial) diabetes insipidus and for the management of the temporary polyuria and polydipsia following head trauma or surgery in the pituitary region. …
— FDA label: Ddavp, Ferring Pharmaceuticals Inc., effective September 28, 2022. Read the full label on DailyMed →
The FDA has 37 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.
This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Boxed warning
A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.
This label has a boxed warning. Read it on the full label →
20 of 37 FDA labels for this medicine have a boxed warning.
Forms and how it is given
What pharmacies pay (NADAC)
The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.
This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.
| Strength and form | Generic or brand | Pharmacies pay |
|---|---|---|
| desmopressin acetate 0.1 mg tablet | Generic | $0.2352 per tablet |
| desmopressin acetate 0.2 mg tablet | Generic | $0.3800 per tablet |
| desmopressin acetate 4 ug/mL injection, solution | Generic | $18.44 per mL |
| desmopressin acetate 4 ug/mL solution | Generic | $18.44 per mL |
| desmopressin acetate 40 ug/10 mL injection, solution | Generic | $18.44 per mL |
NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.
Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →
Companies that list this medicine
Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.
- Nordic Pharma, Inc.7 products
- Ferring Pharmaceuticals Inc.5 products
- Sun Pharmaceutical Industries, Inc.4 products
- UBI Pharma Inc.3 products
- Bryant Ranch Prepack2 products
- Caplin Steriles Limited2 products
- Armas Pharmaceuticals Inc.2 products
- KVK-Tech, Inc.2 products
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.2 products
- Aurobindo Pharma Limited2 products
- BluePoint Laboratories2 products
- Meitheal Pharmaceuticals Inc.2 products
- XGen Pharmaceuticals DJB, Inc.2 products
- American Health Packaging2 products
- Fresenius Kabi USA, LLC2 products
- Gland Pharma Limited2 products
- Sagent Pharmaceuticals2 products
- Avenacy, LLC1 product
- The J. Molner Company LLC1 product
- Apotex Corp.1 product
- Northwind Health Company, LLC1 product
- Remedyrepack Inc.1 product
- Bauch & Lomb Incorporated1 product
- Dr.Reddys Laboratories Inc1 product
- Oceanside Pharmaceuticals1 product
- Dr. Reddy's Laboratories Inc.1 product
- Eton Pharmaceuticals, Inc.1 product
FDA approval history
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Sponsor | Approved | Later changes approved |
|---|---|---|---|
| NDA018938 DDAVP | J Molner | March 30, 1984 | 14, latest July 21, 2022 2022: Labeling · 2018: Labeling · 2015: Labeling |
| NDA019955 DDAVP | Ferring Pharms Inc | September 6, 1995 | 7, latest February 28, 2014 2014: Manufacturing (CMC) · 2007: Labeling · 2005: Labeling |
| NDA020355 STIMATE, STIMATE (NEEDS NO REFRIGERATION) | Ferring Pharms Inc | March 7, 1994 | 11, latest July 15, 2026 2026: Labeling · 2013: Manufacturing (CMC) · 2013: Labeling |
| NDA219873 DESMODA | Eton | February 25, 2026 | — |
Generic approvals (15)
- ANDA074888Meitheal · October 15, 1997
- ANDA074830Bausch · January 25, 1999
- ANDA077414Apotex · March 7, 2006
- ANDA091280Sun Pharm Inds Ltd · January 25, 2013
- ANDA207880Heritage Pharma · May 26, 2017
- ANDA204695Sagent Pharms Inc · August 22, 2017
- ANDA204751Sagent Pharms Inc · August 22, 2017
- ANDA210371Abhai LLC · January 28, 2019
- ANDA210218Ubi · February 14, 2020
- ANDA210223Ubi · September 17, 2020
- ANDA215961DR Reddys · August 19, 2022
- ANDA216922Gland · November 16, 2022
- ANDA216904Gland · March 20, 2023
- ANDA213095Aurobindo Pharma · March 21, 2024
- ANDA219981Caplin · February 27, 2026
Shortage status
The FDA drug shortage list does not show these products.
Recalls
From FDA enforcement reports, matched by the product’s NDC code. A recall usually covers specific lots only: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.
-
November 23, 2022 · Class II · Terminated · D-0072-2023
Subpotent Drug
Desmopressin Acetate Tablets 0.2mg, 100-count bottles, RX Only, Distributed by: Avet Pharmaceuticals Inc. East Brunswick, NJ 08816, NDC 23155-490-01 — Heritage Pharmaceuticals Inc
What do the recall classes mean?
Class I: The most serious type: there is a reasonable chance that using the product will cause serious health problems or death.
Class II: Using the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
Class III: Using the product is not likely to cause health problems (for example a labeling or packaging issue).
Official identifiers
| RxCUI (RxNorm) | 833008, 849501, 849503, 849506, 849515, 849517, 849524, 1723232, 1723234, 1797859 … (+3) |
|---|---|
| SPL set ID of the quoted label | 651f6fee-a2c7-431b-8d5d-58b156c72244 |
| FDA labels (SPL) | 37 |
| FDA applications | NDA018938, NDA019955, NDA020355, NDA219873, 15 ANDA |
| Active ingredients (FDA) | DESMOPRESSIN ACETATE |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Ddavp, Ferring Pharmaceuticals Inc., effective September 28, 2022; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →