Inactive ingredients by manufacturer

Cisatracurium inactive ingredients by manufacturer

Wondering whether your Cisatracurium 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 Cisatracurium 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 38 of the 38 current Cisatracurium products on the market today, from 15 companies listing it with the FDA, and lined them up side by side.

Ask about your bottle

Is there something in your Cisatracurium? 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 Cisatracurium products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseNo checked product

    No checked Cisatracurium product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Cisatracurium product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Cisatracurium product lists soy.

  4. Synthetic dyesNo checked product

    No checked Cisatracurium product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Cisatracurium product lists gelatin.

Also listed by some products: Benzyl alcohol 10 of 38

Find a version without it

Every current Cisatracurium product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
Armas Pharmaceuticals 1 product
200 mg/20 mL injectionNDC 72485-0513-10 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
Avenacy, LLC 1 product
10 mg/mL injectionNDC 83634-0655-20 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
Camber Pharmaceuticals Inc. 3 products
2 mg/mL injectionNDC 31722-0313-10 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
2 mg/mL injectionNDC 31722-0314-10 Benzyl alcohol
Show 3 ingredients

BENZENESULFONIC ACID, BENZYL ALCOHOL, WATER
10 mg/mL injectionNDC 31722-0312-10 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
Caplin Steriles Limited 3 products
2 mg/mL injectionNDC 65145-0135-01 None of these listed
Show 3 ingredients

BENZENESULFONIC ACID, NITROGEN, WATER
2 mg/mL injectionNDC 65145-0136-01 Benzyl alcohol
Show 4 ingredients

BENZENESULFONIC ACID, BENZYL ALCOHOL, NITROGEN, WATER
10 mg/mL injectionNDC 65145-0137-01 None of these listed
Show 3 ingredients

BENZENESULFONIC ACID, NITROGEN, WATER
Eugia US LLC 2 products
10 mg/5 mL injectionNDC 55150-0284-10 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
20 mg/10 mL injectionNDC 55150-0286-10 Benzyl alcohol
Show 3 ingredients

BENZENESULFONIC ACID, BENZYL ALCOHOL, WATER
Fresenius Kabi USA, LLC 3 products
2 mg/mL injectionNDC 63323-0417-10 Benzyl alcohol
Show 2 ingredients

BENZENESULFONIC ACID, BENZYL ALCOHOL
2 mg/mL injectionNDC 63323-0416-05 None of these listed
Show 1 ingredient

BENZENESULFONIC ACID
10 mg/mL injectionNDC 63323-0418-20 None of these listed
Show 1 ingredient

BENZENESULFONIC ACID
Gland Pharma Limited 3 products
2 mg/mL injectionNDC 68083-0486-01 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
2 mg/mL injectionNDC 68083-0488-01 Benzyl alcohol
Show 3 ingredients

BENZENESULFONIC ACID, BENZYL ALCOHOL, WATER
10 mg/mL injectionNDC 68083-0487-01 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
Hikma Pharmaceuticals USA Inc. 3 products
2 mg/mL injectionNDC 00143-9397-10 Benzyl alcohol
Show 3 ingredients

BENZENESULFINIC ACID, BENZYL ALCOHOL, WATER
2 mg/mL injectionNDC 00143-9396-01 None of these listed
Show 2 ingredients

BENZENESULFINIC ACID, WATER
10 mg/mL injectionNDC 00143-9160-10 None of these listed
Show 2 ingredients

BENZENESULFINIC ACID, WATER
Hospira, Inc. 3 products
2 mg/mL injectionNDC 00409-1208-01 Benzyl alcohol
Show 3 ingredients

BENZENESULFONIC ACID, BENZYL ALCOHOL, WATER
2 mg/mL injectionNDC 00409-1098-02 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
10 mg/mL injectionNDC 00409-1103-01 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
Meitheal Pharmaceuticals Inc. 3 products
10 mg/5 mL injectionNDC 71288-0712-06 None of these listed
Show 1 ingredient

BENZENESULFONIC ACID
20 mg/10 mL injectionNDC 71288-0714-11 Benzyl alcohol
Show 2 ingredients

BENZENESULFONIC ACID, BENZYL ALCOHOL
200 mg/20 mL injectionNDC 71288-0713-21 None of these listed
Show 1 ingredient

BENZENESULFONIC ACID
Sandoz Inc 3 products
2 mg/mL injectionNDC 00781-3152-95 Benzyl alcohol
Show 3 ingredients

BENZENESULFONIC ACID, BENZYL ALCOHOL, WATER
2 mg/mL injectionNDC 00781-3150-95 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
10 mg/mL injectionNDC 00781-3153-95 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
Slate Run Pharmaceuticals, LLC 3 products
2 mg/mL injectionNDC 70436-0113-82 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
2 mg/mL injectionNDC 70436-0112-82 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
10 mg/mL injectionNDC 70436-0114-82 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
Somerset Therapeutics, LLC 3 products
2 mg/mL injectionNDC 70069-0161-01 Benzyl alcohol
Show 3 ingredients

BENZENESULFONIC ACID, BENZYL ALCOHOL, WATER
2 mg/mL injectionNDC 70069-0141-01 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
10 mg/mL injectionNDC 70069-0151-01 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
Zydus Pharmaceuticals USA Inc. 2 products
2 mg/mL injectionNDC 70710-1532-06 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
10 mg/mL injectionNDC 70710-1534-06 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
Zydus Lifesciences Limited 2 products
2 mg/mL injectionNDC 72785-0008-06 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, WATER
10 mg/mL injectionNDC 72785-0009-06 None of these listed
Show 2 ingredients

BENZENESULFONIC ACID, 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.

Cisatracurium without benzyl alcohol

Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 10 of 38 checked products list benzyl alcohol; 28 do not.

Does not list benzyl alcohol

Lists benzyl alcohol

At the pharmacy counter

How to use this at the pharmacy counter

  1. 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.
  2. 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.
  3. 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.
  4. 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.
Ask Dr. Staiger which Cisatracurium product suits you →

Common questions about Cisatracurium inactive ingredients

Is Cisatracurium gluten-free?
This page cannot certify any Cisatracurium product gluten-free; it reports what each label declares. Of the 38 products checked, none lists a wheat, barley, rye or gluten ingredient, and none lists a starch without a stated source. If you have celiac disease, ask the manufacturer's medical information line for a written gluten statement for the lot you have.
Does Cisatracurium contain lactose?
No checked Cisatracurium product lists lactose on its label. People with a milk allergy or a strong intolerance often prefer a version that does not list it.
Does Cisatracurium contain soy?
No checked Cisatracurium product lists a soy ingredient (soybean oil or soy lecithin) on its label. Soy lecithin is the usual form and the amount is small, but people with a soy allergy often prefer a version that does not list it.
Is there a dye-free Cisatracurium?
No checked Cisatracurium product lists a synthetic dye (an FD&C or D&C colorant) on its label. Colorants often differ by strength within one company's line, so compare the lists above strength by strength.
Does Cisatracurium contain gelatin?
No checked Cisatracurium product lists gelatin on its label. Gelatin is usually bovine or porcine and the label rarely says which; for kosher, halal or vegetarian needs, ask the manufacturer.
Why do the inactive ingredients differ between manufacturers?
A generic must match the brand's active ingredient, strength and dose form. For injectable, ophthalmic and otic products the FDA generally requires the inactive ingredients to match the reference product as well, so the lists on this page differ less than they do for tablets and capsules; the differences that remain come from the exact product and container each company files.
Can my pharmacy give me a specific manufacturer's version?
Often, if you ask before the prescription is filled: many pharmacies order from wholesalers that carry several companies' versions and can request a particular one. Some pharmacies buy a generic from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check. Give them the NDC from this page; the company name alone is often enough.
How current is this list?
The products are the ones in the FDA's current NDC directory as of October 6, 2026, and each inactive-ingredient list is the manufacturer's FDA label as our label sync last read it. Formulations change, so check the label on your own bottle and ask your pharmacist if a refill looks different.

Sources: the products are the finished Cisatracurium 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 Cisatracurium guide