Esmolol inactive ingredients by manufacturer
Wondering whether your Esmolol 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 Esmolol 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 25 of the 36 current Esmolol products on the market today, from 15 companies listing it with the FDA, and lined them up side by side. 6 are still being read and will appear on a later visit. 5 labels have no inactive-ingredient list we could read, so those products cannot be compared.
Ask about your bottle
Is there something in your Esmolol? 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 Esmolol products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Esmolol product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Esmolol product lists a wheat or gluten source.
-
SoyNo checked product
No checked Esmolol product lists soy.
-
Synthetic dyesNo checked product
No checked Esmolol product lists synthetic dyes.
-
GelatinNo checked product
No checked Esmolol product lists gelatin.
Find a version without it
Every current Esmolol product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Amneal Pharmaceuticals LLC 2 products | ||
| 10 mg/mL injectionNDC 70121-1716-03 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 70121-1717-03 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Baxter Healthcare Company 7 products | ||
| 10 mg/mL injectionNDC 10019-0672-10 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 10 mg/mL injectionNDC 10019-0670-10 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 10 mg/mL injectionNDC 10019-0055-61 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 10 mg/mL injectionNDC 10019-0115-01 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 10019-0668-10 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 10019-0666-10 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 10019-0075-87 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Baxter Healthcare Corporation 1 product | ||
| 10 mg/mL injectionNDC 10019-0120-01 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Eugia US LLC 3 products | ||
| 10 mg/mL injectionNDC 55150-0420-10 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 55150-0421-10 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 100 mg/10 mL injectionNDC 55150-0194-10 | None of these listed |
Show 5 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| Fresenius Kabi USA, LLC 2 products | ||
| 10 mg/mL injectionNDC 63323-0661-14 | Still being read | Not read yet |
| 10 mg/mL injectionNDC 63323-0652-10 | None of these listed |
Show 5 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| Gland Pharma Limited 1 product | ||
| 10 mg/mL injectionNDC 68083-0211-25 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Henry Schein, Inc 1 product | ||
| 10 mg/mL injectionNDC 00404-9825-10 | No inactive-ingredient list on the label | No list we could read |
| Henry Schein, Inc. 2 products | ||
| 10 mg/mL injectionNDC 00404-9785-10 | None of these listed |
Show 5 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE ANHYDROUS, SODIUM HYDROXIDE, WATER |
| 100 mg/10 mL injectionNDC 00404-9858-10 | Still being read | Not read yet |
| HF Acquisition Co LLC, DBA HealthFirst 4 products | ||
| 10 mg/mL injectionNDC 51662-1427-01 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 10 mg/mL injectionNDC 51662-1371-01 | None of these listed |
Show 4 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE |
| 10 mg/mL injectionNDC 51662-1322-01 | None of these listed |
Show 5 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE ANHYDROUS, SODIUM HYDROXIDE, WATER |
| 100 mg/10 mL injectionNDC 51662-1444-01 | None of these listed |
Show 5 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| Medical Purchasing Solutions, LLC 2 products | ||
| 10 mg/mL injectionNDC 71872-7136-01 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 100 mg/10 mL injectionNDC 71872-7049-01 | Still being read | Not read yet |
| Mylan Institutional LLC 3 products | ||
| 10 mg/mL injectionNDC 67457-0657-25 | Still being read | Not read yet |
| 10 mg/mL injectionNDC 67457-0182-10 | None of these listed |
Show 5 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE ANHYDROUS, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 67457-0658-10 | None of these listed |
Show 6 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| ProPharma Distribution 1 product | ||
| 100 mg/10 mL injectionNDC 84549-0194-10 | None of these listed |
Show 5 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| Remedyrepack Inc. 1 product | ||
| 100 mg/10 mL injectionNDC 70518-4410-00 | None of these listed |
Show 5 ingredientsACETIC ACID, HYDROCHLORIC ACID, SODIUM ACETATE, SODIUM HYDROXIDE, WATER |
| Sagent Pharmaceuticals 2 products | ||
| 10 mg/mL injectionNDC 25021-0308-84 | Still being read | Not read yet |
| 20 mg/mL injectionNDC 25021-0309-82 | Still being read | Not read yet |
| WG Critical Care, LLC 4 products | ||
| 10 mg/mL injectionNDC 44567-0811-10 | No inactive-ingredient list on the label | No list we could read |
| 10 mg/mL injectionNDC 44567-0450-10 | No inactive-ingredient list on the label | No list we could read |
| 20 mg/mL injectionNDC 44567-0451-10 | No inactive-ingredient list on the label | No list we could read |
| 20 mg/mL injectionNDC 44567-0812-10 | No inactive-ingredient list on the label | No list we could read |
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.
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 Esmolol inactive ingredients
Is Esmolol gluten-free?
Does Esmolol contain lactose?
Does Esmolol contain soy?
Is there a dye-free Esmolol?
Does Esmolol 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 Esmolol 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 Esmolol guide