Vasopressin inactive ingredients by manufacturer
Wondering whether your Vasopressin 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 Vasopressin 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 30 of the 30 current Vasopressin products on the market today, from 16 companies listing it with the FDA, and lined them up side by side.
Ask about your bottle
Is there something in your Vasopressin? 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 Vasopressin products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Vasopressin product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Vasopressin product lists a wheat or gluten source.
-
SoyNo checked product
No checked Vasopressin product lists soy.
-
Synthetic dyesNo checked product
No checked Vasopressin product lists synthetic dyes.
-
GelatinNo checked product
No checked Vasopressin product lists gelatin.
Also listed by some products: Sugar 3 of 30
Find a version without it
Every current Vasopressin product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| American Regent, Inc. 2 products | ||
| 20 [USP'U]/mL injectionNDC 00517-1020-25 | None of these listed |
Show 4 ingredientsACETIC ACID, CHLOROBUTANOL, SODIUM CHLORIDE, WATER |
| 20 [USP'U]/mL injectionNDC 00517-1030-01 | None of these listed |
Show 4 ingredientsACETIC ACID, CHLOROBUTANOL, SODIUM CHLORIDE, WATER |
| Amneal Pharmaceuticals LLC 1 product | ||
| 20 [USP'U]/mL injectionNDC 70121-1642-02 | None of these listed |
Show 5 ingredientsHYDROCHLORIC ACID, LACTIC ACID, SODIUM HYDROXIDE, SODIUM LACTATE, WATER |
| Amphastar Pharmaceuticals, Inc. 1 product | ||
| 20 [USP'U]/mL injectionNDC 00548-9701-00 | None of these listed |
Show 3 ingredientsACETIC ACID, CHLOROBUTANOL, WATER |
| Baxter Healthcare Corporation 2 products | ||
| 20 [USP'U]/100 mL injectionNDC 00338-9640-12 | None of these listed |
Show 3 ingredientsSODIUM CHLORIDE, SODIUM LACTATE, WATER |
| 40 [USP'U]/100 mL injectionNDC 00338-9647-12 | None of these listed |
Show 3 ingredientsSODIUM CHLORIDE, SODIUM LACTATE, WATER |
| Civica, Inc. 1 product | ||
| 20 [USP'U]/mL injectionNDC 72572-0860-25 | None of these listed |
Show 4 ingredientsACETIC ACID, CHLOROBUTANOL, SODIUM CHLORIDE, WATER |
| Dr. Reddy's Laboratories, Inc. 1 product | ||
| 20 [USP'U]/mL injectionNDC 43598-0914-06 | None of these listed |
Show 4 ingredientsHydrochloric Acid, SODIUM ACETATE, Sodium Hydroxide, WATER |
| Eugia US LLC 1 product | ||
| 20 [USP'U]/mL injectionNDC 55150-0370-01 | None of these listed |
Show 3 ingredientsACETIC ACID, CHLOROBUTANOL, WATER |
| Fresenius Kabi USA, LLC 2 products | ||
| 20 [USP'U]/mL injectionNDC 65219-0039-01 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| 20 [USP'U]/mL injectionNDC 63323-0930-01 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| Gland Pharma Limited 2 products | ||
| 0.4 [USP'U]/mL injectionNDC 68083-0663-10 | Sugar (sucrose, dextrose) |
Show 6 ingredientsACETIC ACID, ANHYDROUS DEXTROSE, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| 20 [USP'U]/mL injectionNDC 68083-0520-10 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| HF Acquisition Co LLC, DBA HealthFirst 5 products | ||
| 20 [USP'U]/mL injectionNDC 51662-1694-02 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| 20 [USP'U]/mL injectionNDC 51662-1623-01 | None of these listed |
Show 3 ingredientsACETIC ACID, CHLOROBUTANOL, WATER |
| 20 [USP'U]/mL injectionNDC 51662-1314-01 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| 20 [USP'U]/mL injectionNDC 51662-1682-01 | None of these listed |
Show 4 ingredientsACETIC ACID, CHLOROBUTANOL, SODIUM CHLORIDE, WATER |
| 20 [USP'U]/mL injectionNDC 51662-1688-01 | None of these listed |
Show 4 ingredientsACETIC ACID, CHLOROBUTANOL, SODIUM CHLORIDE, WATER |
| Long Grove Pharmaceuticals, LLC 2 products | ||
| 0.2 [USP'U]/mL injectionNDC 81298-8552-03 | None of these listed |
Show 5 ingredientsASPARTIC ACID, BORIC ACID, CHLOROBUTANOL, SODIUM CHLORIDE, WATER |
| 0.4 [USP'U]/mL injectionNDC 81298-8554-03 | None of these listed |
Show 5 ingredientsASPARTIC ACID, BORIC ACID, CHLOROBUTANOL, SODIUM CHLORIDE, WATER |
| Medical Purchasing Solutions, LLC 3 products | ||
| 20 [USP'U]/mL injectionNDC 71872-7334-01 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| 20 [USP'U]/mL injectionNDC 71872-7264-01 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| 20 [USP'U]/mL injectionNDC 71872-7306-01 | None of these listed |
Show 3 ingredientsACETIC ACID, CHLOROBUTANOL, WATER |
| Medical Purchasin Solutions, LLC 1 product | ||
| 20 [USP'U]/mL injectionNDC 71872-7014-01 | None of these listed |
Show 2 ingredientsSODIUM ACETATE, WATER |
| Par Health USA, LLC 4 products | ||
| 0.2 [USP'U]/mL injectionNDC 42023-0237-10 | Sugar (sucrose, dextrose) |
Show 6 ingredientsACETIC ACID, DEXTROSE, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| 0.4 [USP'U]/mL injectionNDC 42023-0219-10 | Sugar (sucrose, dextrose) |
Show 6 ingredientsACETIC ACID, DEXTROSE, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| 20 [USP'U]/mL injectionNDC 42023-0164-10 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| 20 [USP'U]/mL injectionNDC 42023-0190-01 | None of these listed |
Show 5 ingredientsCHLOROBUTANOL, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| ProPharma Distribution 1 product | ||
| 20 [USP'U]/mL injectionNDC 84549-0370-25 | None of these listed |
Show 3 ingredientsACETIC ACID, CHLOROBUTANOL, WATER |
| Sagent Pharmaceuticals 1 product | ||
| 20 [USP'U]/mL injectionNDC 25021-0474-01 | None of these listed |
Show 4 ingredientsHydrochloric Acid, Sodium Acetate, Sodium Hydroxide, Water |
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.
Vasopressin without sugar (sucrose or dextrose)
Sugar (sucrose, dextrose): A consideration in diabetes, mostly in liquids and chewables. 3 of 30 checked products list sugar (sucrose or dextrose); 27 do not.
Does not list sugar (sucrose or dextrose)
- American Regent: 20 [USP'U]/mL injection (NDC 00517-1020-25), 20 [USP'U]/mL injection (NDC 00517-1030-01)
- Amneal: 20 [USP'U]/mL injection
- Amphastar: 20 [USP'U]/mL injection
- Baxter Healthcare: 20 [USP'U]/100 mL injection, 40 [USP'U]/100 mL injection
- Civica: 20 [USP'U]/mL injection
- Dr. Reddy's: 20 [USP'U]/mL injection
- Eugia: 20 [USP'U]/mL injection
- Fresenius Kabi: 20 [USP'U]/mL injection (NDC 65219-0039-01), 20 [USP'U]/mL injection (NDC 63323-0930-01)
- Gland: 20 [USP'U]/mL injection
- HF Acquisition Co LLC, DBA HealthFirst: 20 [USP'U]/mL injection (NDC 51662-1694-02), 20 [USP'U]/mL injection (NDC 51662-1623-01), 20 [USP'U]/mL injection (NDC 51662-1314-01), 20 [USP'U]/mL injection (NDC 51662-1682-01), 20 [USP'U]/mL injection (NDC 51662-1688-01)
- Long Grove: 0.2 [USP'U]/mL injection, 0.4 [USP'U]/mL injection
- Medical Purchasing Solutions: 20 [USP'U]/mL injection (NDC 71872-7334-01), 20 [USP'U]/mL injection (NDC 71872-7264-01), 20 [USP'U]/mL injection (NDC 71872-7306-01)
- Medical Purchasin Solutions: 20 [USP'U]/mL injection
- Par Health: 20 [USP'U]/mL injection (NDC 42023-0164-10), 20 [USP'U]/mL injection (NDC 42023-0190-01)
- ProPharma Distribution: 20 [USP'U]/mL injection
- Sagent: 20 [USP'U]/mL injection
Lists sugar (sucrose or dextrose)
- Gland: 0.4 [USP'U]/mL injection
- Par Health: 0.2 [USP'U]/mL injection, 0.4 [USP'U]/mL injection
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 Vasopressin inactive ingredients
Is Vasopressin gluten-free?
Does Vasopressin contain lactose?
Does Vasopressin contain soy?
Is there a dye-free Vasopressin?
Does Vasopressin 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 Vasopressin 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 Vasopressin guide