Etomidate inactive ingredients by manufacturer
Wondering whether your Etomidate 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 Etomidate 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 19 of the 24 current Etomidate products on the market today, from 12 companies listing it with the FDA, and lined them up side by side. 5 are still being read and will appear on a later visit.
Ask about your bottle
Is there something in your Etomidate? 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 Etomidate products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Etomidate product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Etomidate product lists a wheat or gluten source.
-
SoyNo checked product
No checked Etomidate product lists soy.
-
Synthetic dyesNo checked product
No checked Etomidate product lists synthetic dyes.
-
GelatinNo checked product
No checked Etomidate product lists gelatin.
Also listed by some products: Propylene glycol 18 of 19
Find a version without it
Every current Etomidate product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Armas Pharmaceuticals Inc. 2 products | ||
| 2 mg/mL injectionNDC 72485-0508-10 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| 2 mg/mL injectionNDC 72485-0509-10 | Still being read | Not read yet |
| Caplin Steriles Limited 2 products | ||
| 2 mg/mL injectionNDC 65145-0127-10 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| 2 mg/mL injectionNDC 65145-0128-10 | Still being read | Not read yet |
| Civica, Inc. 2 products | ||
| 2 mg/mL injectionNDC 72572-0161-10 | Still being read | Not read yet |
| 2 mg/mL injectionNDC 72572-0160-10 | Propylene glycol |
Show 1 ingredientPROPYLENE GLYCOL |
| Eugia US LLC 2 products | ||
| 20 mg/10 mL injectionNDC 55150-0221-10 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| 40 mg/20 mL injectionNDC 55150-0222-20 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| Fosun Pharma USA Inc 2 products | ||
| 2 mg/mL injectionNDC 72266-0147-10 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| 2 mg/mL injectionNDC 72266-0146-10 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| Fresenius Kabi USA, LLC 2 products | ||
| 2 mg/mL injectionNDC 65219-0447-20 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| 2 mg/mL injectionNDC 65219-0445-10 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| Gland Pharma Limited 2 products | ||
| 2 mg/mL injectionNDC 68083-0235-10 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| 2 mg/mL injectionNDC 68083-0234-10 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| Henry Schein, Inc. 1 product | ||
| 2 mg/mL injectionNDC 00404-9811-10 | None of these listed |
Show 1 ingredientWATER |
| HF Acquisition Co LLC, DBA HealthFirst 2 products | ||
| 2 mg/mL injectionNDC 51662-1485-01 | Propylene glycol |
Show 1 ingredientPROPYLENE GLYCOL |
| 40 mg/20 mL injectionNDC 51662-1542-01 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| Hikma Pharmaceuticals USA Inc. 4 products | ||
| 2 mg/mL injectionNDC 00143-9310-10 | Propylene glycol |
Show 1 ingredientPROPYLENE GLYCOL |
| 2 mg/mL injectionNDC 00143-9311-10 | Still being read | Not read yet |
| 2 mg/mL injectionNDC 00143-9506-10 | Propylene glycol |
Show 1 ingredientPROPYLENE GLYCOL |
| 2 mg/mL injectionNDC 00143-9507-10 | Propylene glycol |
Show 1 ingredientPROPYLENE GLYCOL |
| Hospira, Inc. 1 product | ||
| 2 mg/mL injectionNDC 00409-6695-01 | Propylene glycol |
Show 2 ingredientsPROPYLENE GLYCOL, WATER |
| Mylan Institutional LLC 2 products | ||
| 2 mg/mL injectionNDC 67457-0902-10 | Still being read | Not read yet |
| 2 mg/mL injectionNDC 67457-0903-20 | Propylene glycol |
Show 1 ingredientPROPYLENE GLYCOL |
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.
Etomidate without propylene glycol
Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 18 of 19 checked products list propylene glycol; 1 does not.
Does not list propylene glycol
- Henry Schein: 2 mg/mL injection
Lists propylene glycol
- Armas: 2 mg/mL injection
- Caplin Steriles: 2 mg/mL injection
- Civica: 2 mg/mL injection
- Eugia: 20 mg/10 mL injection, 40 mg/20 mL injection
- Fosun: 2 mg/mL injection (NDC 72266-0147-10), 2 mg/mL injection (NDC 72266-0146-10)
- Fresenius Kabi: 2 mg/mL injection (NDC 65219-0447-20), 2 mg/mL injection (NDC 65219-0445-10)
- Gland: 2 mg/mL injection (NDC 68083-0235-10), 2 mg/mL injection (NDC 68083-0234-10)
- HF Acquisition Co LLC, DBA HealthFirst: 2 mg/mL injection, 40 mg/20 mL injection
- Hikma: 2 mg/mL injection (NDC 00143-9310-10), 2 mg/mL injection (NDC 00143-9506-10), 2 mg/mL injection (NDC 00143-9507-10)
- Hospira: 2 mg/mL injection
- Mylan Institutional: 2 mg/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 Etomidate inactive ingredients
Is Etomidate gluten-free?
Does Etomidate contain lactose?
Does Etomidate contain soy?
Is there a dye-free Etomidate?
Does Etomidate 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 Etomidate 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 Etomidate guide