Cytarabine inactive ingredients by manufacturer
Wondering whether your Cytarabine 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 Cytarabine 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 11 of the 14 current Cytarabine products on the market today, from 5 companies listing it with the FDA, and lined them up side by side. 3 are still being read and will appear on a later visit.
Ask about your bottle
Is there something in your Cytarabine? 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 Cytarabine products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Cytarabine product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Cytarabine product lists a wheat or gluten source.
-
SoyNo checked product
No checked Cytarabine product lists soy.
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Synthetic dyesNo checked product
No checked Cytarabine product lists synthetic dyes.
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GelatinNo checked product
No checked Cytarabine product lists gelatin.
Also listed by some products: Benzyl alcohol 2 of 11
Find a version without it
Every current Cytarabine product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Fresenius Kabi USA, LLC 1 product | ||
| 100 mg/mL injectionNDC 63323-0120-20 | None of these listed |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM HYDROXIDE, WATER |
| Gland Pharma Limited 2 products | ||
| 20 mg/mL injectionNDC 68083-0343-05 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 100 mg/mL injectionNDC 68083-0337-01 | Still being read | Not read yet |
| Hospira, Inc. 5 products | ||
| 20 mg/mL injectionNDC 61703-0304-36 | Benzyl alcohol |
Show 4 ingredientsBENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 61703-0305-38 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 61703-0303-46 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 100 mg/mL injectionNDC 61703-0319-22 | Still being read | Not read yet |
| 100 mg/mL injectionNDC 61703-0155-01 | None of these listed |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM HYDROXIDE, WATER |
| Meitheal Pharmaceuticals Inc. 4 products | ||
| 2 g/20 mL injectionNDC 71288-0109-20 | Still being read | Not read yet |
| 20 mg/mL injectionNDC 71288-0169-25 | Benzyl alcohol |
Show 4 ingredientsbenzyl alcohol, hydrochloric acid, sodium hydroxide, water |
| 20 mg/mL injectionNDC 71288-0168-50 | None of these listed |
Show 4 ingredientshydrochloric acid, sodium chloride, sodium hydroxide, water |
| 20 mg/mL injectionNDC 71288-0108-06 | None of these listed |
Show 4 ingredientshydrochloric acid, sodium chloride, sodium hydroxide, water |
| Sagent Pharmaceuticals 2 products | ||
| 20 mg/mL injectionNDC 25021-0229-05 | None of these listed |
Show 4 ingredientshydrochloric acid, sodium chloride, sodium hydroxide, water |
| 100 mg/mL injectionNDC 25021-0223-20 | None of these listed |
Show 3 ingredientshydrochloric acid, 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.
Cytarabine without benzyl alcohol
Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 2 of 11 checked products list benzyl alcohol; 9 do not.
Does not list benzyl alcohol
- Fresenius Kabi: 100 mg/mL injection
- Gland: 20 mg/mL injection
- Hospira: 20 mg/mL injection (NDC 61703-0305-38), 20 mg/mL injection (NDC 61703-0303-46), 100 mg/mL injection
- Meitheal: 20 mg/mL injection (NDC 71288-0168-50), 20 mg/mL injection (NDC 71288-0108-06)
- Sagent: 20 mg/mL injection, 100 mg/mL injection
Lists benzyl alcohol
- Hospira: 20 mg/mL injection
- Meitheal: 20 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 Cytarabine inactive ingredients
Is Cytarabine gluten-free?
Does Cytarabine contain lactose?
Does Cytarabine contain soy?
Is there a dye-free Cytarabine?
Does Cytarabine 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 Cytarabine products in the FDA's current NDC directory (openFDA), as of October 5, 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 Cytarabine guide