Desmopressin inactive ingredients by manufacturer
Wondering whether your Desmopressin has lactose, gluten, soy, a dye or gelatin in it? The medicine is the same, but the fillers, coatings and colors differ from one company to the next. This page shows what each Desmopressin product's FDA label lists, so you can find a version that leaves out what you avoid and ask your pharmacist for it by its NDC.
We have read the FDA labels of 53 of the 55 current Desmopressin products on the market today, from 29 companies listing it with the FDA, and lined them up side by side. 2 labels have no inactive-ingredient list we could read, so those products cannot be compared.
Ask about your bottle
Is there something in your Desmopressin? Ask in plain words.
Name the company, strength or the NDC on your bottle and the ingredient you avoid. The answer comes only from the FDA labels on this page.
Answers are drawn from the FDA label data on this page and checked against it. They are not medical advice: confirm with your pharmacist before relying on them.
The short answer
Which Desmopressin products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseDiffers by manufacturer
22 of 53 checked products list lactose; 31 do not. See the products
-
Wheat or gluten sourceNo checked product
No checked Desmopressin product lists a wheat or gluten source.
-
SoyNo checked product
No checked Desmopressin product lists soy.
-
Synthetic dyesNo checked product
No checked Desmopressin product lists synthetic dyes.
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GelatinNo checked product
No checked Desmopressin product lists gelatin.
Also listed by some products: Corn 15 of 53
Find a version without it
Every current Desmopressin product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| American Health Packaging 2 products | ||
| 0.1 mg tabletNDC 60687-0721-21 | Lactose Corn-derived |
Show 3 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, STARCH, CORN |
| 0.2 mg tabletNDC 60687-0732-21 | Lactose Corn-derived |
Show 3 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, STARCH, CORN |
| Apotex Corp. 3 products | ||
| 10 mcg nasal sprayNDC 60505-0815-00 | None of these listed |
Show 5 ingredientsBENZALKONIUM CHLORIDE, CITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, WATER |
| 0.1 mg tabletNDC 60505-0257-01 | Lactose Corn-derived |
Show 3 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, STARCH, CORN |
| 0.2 mg tabletNDC 60505-0258-01 | Lactose Corn-derived |
Show 3 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, STARCH, CORN |
| Armas Pharmaceuticals Inc. 2 products | ||
| 4 mcg/mL injectionNDC 72485-0523-10 | None of these listed |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| 40 mcg/10 mL injectionNDC 72485-0524-01 | None of these listed |
Show 4 ingredientsCHLOROBUTANOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| Aurobindo Pharma Limited 2 products | ||
| 0.1 mg tabletNDC 59651-0249-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE K30, STARCH, CORN |
| 0.2 mg tabletNDC 59651-0250-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE K30, STARCH, CORN |
| Avenacy, Inc. 1 product | ||
| 4 mcg/mL injectionNDC 83634-0451-01 | None of these listed |
Show 3 ingredientschlorobutanol hemihydrate, hydrochloric acid, sodium chloride |
| Bauch & Lomb Incorporated 1 product | ||
| 0.1 mg/mL nasal sprayNDC 24208-0342-05 | None of these listed |
Show 4 ingredientsCHLOROBUTANOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| BluePoint Laboratories 2 products | ||
| 0.1 mg tabletNDC 68001-0574-00 | Lactose Corn-derived |
Show 3 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, STARCH, CORN |
| 0.2 mg tabletNDC 68001-0575-00 | Lactose Corn-derived |
Show 3 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, STARCH, CORN |
| Bryant Ranch Prepack 2 products | ||
| 0.2 mg tabletNDC 63629-3257-01 | Lactose Corn-derived |
Show 3 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, STARCH, CORN |
| 0.2 mg tabletNDC 71335-2342-01 | Lactose |
Show 4 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, POVIDONE, UNSPECIFIED, STARCH, POTATO |
| Caplin Steriles Limited 2 products | ||
| 4 mcg/mL injectionNDC 65145-0184-01 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL, HYDROCHLORIC ACID, SODIUM CHLORIDE |
| 4 mcg/mL injectionNDC 65145-0183-10 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL, HYDROCHLORIC ACID, SODIUM CHLORIDE |
| Dr. Reddy's Laboratories Inc. 1 product | ||
| 4 mcg/mL injectionNDC 43598-0053-11 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL, HYDROCHLORIC ACID, SODIUM CHLORIDE |
| Dr.Reddys' Laboratories Inc 1 product | ||
| 4 mcg/mL injectionNDC 43598-0931-09 | No inactive-ingredient list on the label | No list we could read |
| Eton Pharmaceuticals, Inc. 1 product | ||
| 0.05 mg/mL oral solutionNDC 71863-0123-14 | None of these listed |
Show 3 ingredientsBENZOIC ACID, SODIUM BENZOATE, WATER |
| Ferring Pharmaceuticals Inc. 5 products | ||
| 4 mcg/mL injectionNDC 55566-2200-00 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL, HYDROCHLORIC ACID, SODIUM CHLORIDE |
| 4 mcg/mL injectionNDC 55566-2300-00 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL, HYDROCHLORIC ACID, SODIUM CHLORIDE |
| 1.5 mg/mL nasal sprayNDC 55566-3000-00 | None of these listed |
Show 5 ingredientsBENZALKONIUM CHLORIDE, CITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE DIBASIC DIHYDRATE, WATER |
| 0.1 mg tabletNDC 55566-2600-00 | Lactose |
Show 4 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, POVIDONE, UNSPECIFIED, STARCH, POTATO |
| 0.2 mg tabletNDC 55566-2700-00 | Lactose |
Show 4 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, POVIDONE, UNSPECIFIED, STARCH, POTATO |
| Fresenius Kabi USA, LLC 2 products | ||
| 4 mcg/mL injectionNDC 65219-0293-01 | None of these listed |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| 4 mcg/mL injectionNDC 65219-0295-10 | None of these listed |
Show 4 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| Gland Pharma Limited 2 products | ||
| 4 mcg/mL injectionNDC 68083-0549-01 | None of these listed |
Show 4 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| 4 mcg/mL injectionNDC 68083-0550-10 | None of these listed |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| Glenmark Pharmaceuticals Inc.,USA 2 products | ||
| 0.1 mg tabletNDC 68462-0275-01 | Lactose |
Show 5 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE, UNSPECIFIED, STARCH, POTATO, TALC |
| 0.2 mg tabletNDC 68462-0276-01 | Lactose |
Show 5 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE, UNSPECIFIED, STARCH, POTATO, TALC |
| Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 2 products | ||
| 0.1 mg tabletNDC 23155-0489-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE K30, STARCH, CORN |
| 0.2 mg tabletNDC 23155-0490-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE K30, STARCH, CORN |
| Kvk-tech, Inc. 2 products | ||
| 0.1 mg tabletNDC 10702-0169-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE, STARCH, CORN |
| 0.2 mg tabletNDC 10702-0170-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE, STARCH, CORN |
| Meitheal Pharmaceuticals Inc. 2 products | ||
| 4 mcg/mL injectionNDC 71288-0440-02 | None of these listed |
Show 4 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| 4 mcg/mL injectionNDC 71288-0441-10 | None of these listed |
Show 4 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| Nordic Pharma, Inc. 4 products | ||
| 4 mcg/mL injectionNDC 69918-0899-01 | None of these listed |
Show 2 ingredientsHydrochloric Acid, Sodium Chloride |
| 4 mcg/mL injectionNDC 69918-0901-10 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL, HYDROCHLORIC ACID, SODIUM CHLORIDE |
| 0.1 mg tabletNDC 69918-0101-01 | Lactose |
Show 4 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, POVIDONE, UNSPECIFIED, STARCH, POTATO |
| 0.2 mg tabletNDC 69918-0201-01 | Lactose |
Show 4 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, POVIDONE, UNSPECIFIED, STARCH, POTATO |
| Northwind Health Company, LLC 1 product | ||
| 0.2 mg tabletNDC 51655-0461-52 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE, STARCH, CORN |
| Oceanside Pharmaceuticals 1 product | ||
| 0.1 mg/mL nasal sprayNDC 68682-0342-05 | None of these listed |
Show 4 ingredientsCHLOROBUTANOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| Remedyrepack Inc. 1 product | ||
| 0.1 mg tabletNDC 70518-4612-00 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE K30, STARCH, CORN |
| Sagent Pharmaceuticals 2 products | ||
| 4 mcg/mL injectionNDC 25021-0460-01 | None of these listed |
Show 2 ingredientshydrochloric acid, sodium chloride |
| 40 mcg/10 mL injectionNDC 25021-0461-10 | None of these listed |
Show 3 ingredientschlorobutanol, hydrochloric acid, sodium chloride |
| Sun Pharmaceutical Industries, Inc. 1 product | ||
| 4 mcg/mL injectionNDC 62756-0529-26 | None of these listed |
Show 4 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| Sun Pharmaceutical Industries Limited 2 products | ||
| 4 mcg/mL injectionNDC 70095-0031-01 | None of these listed |
Show 4 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| 4 mcg/mL injectionNDC 70095-0026-02 | None of these listed |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, WATER |
| The J. Molner Company LLC 1 product | ||
| 4 mcg/mL injectionNDC 83148-0126-01 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE |
| UBI Pharma Inc. 3 products | ||
| 4 mcg/mL injectionNDC 72843-0461-10 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE |
| 4 mcg/mL injectionNDC 72843-0459-10 | No inactive-ingredient list on the label | No list we could read |
| 40 mcg/10 mL injectionNDC 72843-0440-01 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE |
| XGen Pharmaceuticals DJB, Inc. 2 products | ||
| 4 mcg/mL injectionNDC 39822-6200-02 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE |
| 4 mcg/mL injectionNDC 39822-6250-01 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL HEMIHYDRATE, HYDROCHLORIC ACID, SODIUM CHLORIDE |
A product with none of these listed is not certified to be without them: the label says what the manufacturer declared, and the source of a starch or a flavor is often not stated. The companies are the FDA's labelers, which include repackagers and distributors selling another company's product under their own label. The NDC opens the product's own page, with the full label and its inactive-ingredient notes.
Desmopressin without lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 22 of 53 checked products list lactose; 31 do not.
Does not list lactose
- Apotex: 10 mcg nasal spray
- Armas: 4 mcg/mL injection, 40 mcg/10 mL injection
- Avenacy: 4 mcg/mL injection
- Bauch & Lomb: 0.1 mg/mL nasal spray
- Caplin Steriles: 4 mcg/mL injection (NDC 65145-0184-01), 4 mcg/mL injection (NDC 65145-0183-10)
- Dr. Reddy's: 4 mcg/mL injection
- Eton: 0.05 mg/mL oral solution
- Ferring: 4 mcg/mL injection (NDC 55566-2200-00), 4 mcg/mL injection (NDC 55566-2300-00), 1.5 mg/mL nasal spray
- Fresenius Kabi: 4 mcg/mL injection (NDC 65219-0293-01), 4 mcg/mL injection (NDC 65219-0295-10)
- Gland: 4 mcg/mL injection (NDC 68083-0549-01), 4 mcg/mL injection (NDC 68083-0550-10)
- Meitheal: 4 mcg/mL injection (NDC 71288-0440-02), 4 mcg/mL injection (NDC 71288-0441-10)
- Nordic: 4 mcg/mL injection (NDC 69918-0899-01), 4 mcg/mL injection (NDC 69918-0901-10)
- Oceanside: 0.1 mg/mL nasal spray
- Sagent: 4 mcg/mL injection, 40 mcg/10 mL injection
- Sun Pharmaceutical Industries, Inc.: 4 mcg/mL injection
- Sun Pharmaceutical Industries Limited: 4 mcg/mL injection (NDC 70095-0031-01), 4 mcg/mL injection (NDC 70095-0026-02)
- The J. Molner: 4 mcg/mL injection
- UBI: 4 mcg/mL injection, 40 mcg/10 mL injection
- XGen Pharmaceuticals DJB: 4 mcg/mL injection (NDC 39822-6200-02), 4 mcg/mL injection (NDC 39822-6250-01)
Lists lactose
- American Health Packaging: 0.1 mg tablet, 0.2 mg tablet
- Apotex: 0.1 mg tablet, 0.2 mg tablet
- Aurobindo: 0.1 mg tablet, 0.2 mg tablet
- BluePoint: 0.1 mg tablet, 0.2 mg tablet
- Bryant Ranch Prepack: 0.2 mg tablet (NDC 63629-3257-01), 0.2 mg tablet (NDC 71335-2342-01)
- Ferring: 0.1 mg tablet, 0.2 mg tablet
- Glenmark: 0.1 mg tablet, 0.2 mg tablet
- Heritage Pharmaceuticals Inc. d/b/a Avet: 0.1 mg tablet, 0.2 mg tablet
- Kvk-tech: 0.1 mg tablet, 0.2 mg tablet
- Nordic: 0.1 mg tablet, 0.2 mg tablet
- Northwind Health: 0.2 mg tablet
- Remedyrepack: 0.1 mg tablet
Desmopressin without corn-derived ingredients
Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. 15 of 53 checked products list corn-derived ingredients; 38 do not.
Does not list corn-derived ingredients
- Apotex: 10 mcg nasal spray
- Armas: 4 mcg/mL injection, 40 mcg/10 mL injection
- Avenacy: 4 mcg/mL injection
- Bauch & Lomb: 0.1 mg/mL nasal spray
- Bryant Ranch Prepack: 0.2 mg tablet
- Caplin Steriles: 4 mcg/mL injection (NDC 65145-0184-01), 4 mcg/mL injection (NDC 65145-0183-10)
- Dr. Reddy's: 4 mcg/mL injection
- Eton: 0.05 mg/mL oral solution
- Ferring: 4 mcg/mL injection (NDC 55566-2200-00), 4 mcg/mL injection (NDC 55566-2300-00), 1.5 mg/mL nasal spray, 0.1 mg tablet, 0.2 mg tablet
- Fresenius Kabi: 4 mcg/mL injection (NDC 65219-0293-01), 4 mcg/mL injection (NDC 65219-0295-10)
- Gland: 4 mcg/mL injection (NDC 68083-0549-01), 4 mcg/mL injection (NDC 68083-0550-10)
- Glenmark: 0.1 mg tablet, 0.2 mg tablet
- Meitheal: 4 mcg/mL injection (NDC 71288-0440-02), 4 mcg/mL injection (NDC 71288-0441-10)
- Nordic: 4 mcg/mL injection (NDC 69918-0899-01), 4 mcg/mL injection (NDC 69918-0901-10), 0.1 mg tablet, 0.2 mg tablet
- Oceanside: 0.1 mg/mL nasal spray
- Sagent: 4 mcg/mL injection, 40 mcg/10 mL injection
- Sun Pharmaceutical Industries, Inc.: 4 mcg/mL injection
- Sun Pharmaceutical Industries Limited: 4 mcg/mL injection (NDC 70095-0031-01), 4 mcg/mL injection (NDC 70095-0026-02)
- The J. Molner: 4 mcg/mL injection
- UBI: 4 mcg/mL injection, 40 mcg/10 mL injection
- XGen Pharmaceuticals DJB: 4 mcg/mL injection (NDC 39822-6200-02), 4 mcg/mL injection (NDC 39822-6250-01)
Lists corn-derived ingredients
- American Health Packaging: 0.1 mg tablet, 0.2 mg tablet
- Apotex: 0.1 mg tablet, 0.2 mg tablet
- Aurobindo: 0.1 mg tablet, 0.2 mg tablet
- BluePoint: 0.1 mg tablet, 0.2 mg tablet
- Bryant Ranch Prepack: 0.2 mg tablet
- Heritage Pharmaceuticals Inc. d/b/a Avet: 0.1 mg tablet, 0.2 mg tablet
- Kvk-tech: 0.1 mg tablet, 0.2 mg tablet
- Northwind Health: 0.2 mg tablet
- Remedyrepack: 0.1 mg tablet
At the pharmacy counter
How to use this at the pharmacy counter
- Pick the company whose list suits you and copy the NDC from the table. Many pharmacies order from wholesalers that carry several companies' versions and can request a particular one if you ask before the prescription is filled; some buy from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check.
- Treat "does not list" as exactly that. The label is what the manufacturer declared; a flavor or a starch may have an unstated source, and lines change. For celiac disease or a serious allergy, ask the manufacturer's medical information line for a written statement about the lot you have.
- Check the bottle each refill. A different company usually means a different shape, color and inactive-ingredient list; the pharmacist can tell you who made it, and the two-NDC comparison shows the difference line by line.
- If you need one company's version kept constant, ask your prescriber to write that company or the NDC on the prescription and tell the pharmacy you need it held. Rules vary by state and plan, so confirm with the pharmacist.
Common questions about Desmopressin inactive ingredients
Is Desmopressin gluten-free?
Does Desmopressin contain lactose?
Does Desmopressin contain soy?
Is there a dye-free Desmopressin?
Does Desmopressin contain gelatin?
Why do the inactive ingredients differ between manufacturers?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Desmopressin products in the FDA's current NDC directory (openFDA), as of October 6, 2026; each inactive-ingredient list is the manufacturer's FDA Structured Product Label via DailyMed, as our label sync last read it. The concern groups are HelloPharmacist's classification of the names the label declares. Educational information only, not medical advice; confirm with your pharmacist before relying on a list. ← Back to the Desmopressin guide