Inactive ingredients by manufacturer

Acalabrutinib inactive ingredients by manufacturer

Wondering whether your Acalabrutinib 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 Acalabrutinib 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 3 of the 3 current Acalabrutinib products on the market today, from 1 company listing it with the FDA, and lined them up side by side.

Ask about your bottle

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

  1. LactoseNo checked product

    No checked Acalabrutinib product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Acalabrutinib product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Acalabrutinib product lists soy.

  4. Synthetic dyesDiffers by manufacturer

    1 of 3 checked products list synthetic dyes; 2 do not. See the products

    Does not list it AstraZeneca
    Lists it AstraZeneca
  5. GelatinDiffers by manufacturer

    1 of 3 checked products list gelatin; 2 do not. See the products

    Does not list it AstraZeneca
    Lists it AstraZeneca

Also listed by some products: Corn 1 of 3 Titanium dioxide 3 of 3 PEG or polysorbate 2 of 3 Sorbitol or mannitol 2 of 3

Find a version without it

Every current Acalabrutinib product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
AstraZeneca Pharmaceuticals LP 3 products
100 mg capsuleNDC 00310-0512-60 Corn-derived Synthetic dyes Titanium dioxide Gelatin
Show 9 ingredients

FD&C BLUE NO. 2, FERRIC OXIDE YELLOW, GELATIN, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE, SODIUM STARCH GLYCOLATE TYPE A POTATO, STARCH, CORN, TITANIUM DIOXIDE
100 mg tabletNDC 00310-3512-60 Titanium dioxide Polyethylene glycol or polysorbate Sorbitol or mannitol
Show 12 ingredients

COPOVIDONE K25-31, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE, UNSPECIFIED, LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED, MANNITOL, MEDIUM-CHAIN TRIGLYCERIDES, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, SODIUM STEARYL FUMARATE, TITANIUM DIOXIDE, WATER
100 mg tabletNDC 00310-4513-60 Titanium dioxide Polyethylene glycol or polysorbate Sorbitol or mannitol
Show 12 ingredients

COPOVIDONE K25-31, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE, UNSPECIFIED, LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED, MANNITOL, MEDIUM-CHAIN TRIGLYCERIDES, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, SODIUM STEARYL FUMARATE, TITANIUM DIOXIDE, 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.

Acalabrutinib without synthetic dyes

Synthetic dyes: FD&C or D&C colorants and their aluminum lakes. 1 of 3 checked products list synthetic dyes; 2 do not.

Does not list synthetic dyes

Lists synthetic dyes

Acalabrutinib without gelatin

Gelatin: animal-derived (usually bovine or porcine); a concern for vegetarian, kosher or halal needs. 1 of 3 checked products list gelatin; 2 do not.

Does not list gelatin

Lists gelatin

Acalabrutinib without corn-derived ingredients

Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. 1 of 3 checked products list corn-derived ingredients; 2 do not.

Does not list corn-derived ingredients

Lists corn-derived ingredients

Acalabrutinib and titanium dioxide

Titanium dioxide: A white colorant some people choose to avoid. Every checked Acalabrutinib product (3) lists titanium dioxide.

Lists titanium dioxide

Acalabrutinib without polyethylene glycol or polysorbate

Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. 2 of 3 checked products list polyethylene glycol or polysorbate; 1 does not.

Does not list polyethylene glycol or polysorbate

Lists polyethylene glycol or polysorbate

Acalabrutinib without sorbitol or mannitol

Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 2 of 3 checked products list sorbitol or mannitol; 1 does not.

Does not list sorbitol or mannitol

Lists sorbitol or mannitol

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 Acalabrutinib product suits you →

Common questions about Acalabrutinib inactive ingredients

Is Acalabrutinib gluten-free?
This page cannot certify any Acalabrutinib product gluten-free; it reports what each label declares. Of the 3 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 Acalabrutinib contain lactose?
No checked Acalabrutinib product lists lactose on its label. The lactose in a tablet or capsule is a small amount, but people with a milk allergy or a strong intolerance often prefer a version that does not list it.
Does Acalabrutinib contain soy?
No checked Acalabrutinib 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 Acalabrutinib?
1 of 3 checked Acalabrutinib products list a synthetic dye (an FD&C or D&C colorant); 2 do not: AstraZeneca (100 mg tablet). Colorants often differ by strength within one company's line, so compare the lists above strength by strength.
Does Acalabrutinib contain gelatin?
1 of 3 checked Acalabrutinib products list gelatin; 2 do not: AstraZeneca (100 mg tablet). 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, dose form and how it is absorbed; its fillers, binders, coatings and colorants are the manufacturer's own choice. That is why one Acalabrutinib product can list lactose and a dye while another from a different company lists neither.
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 Acalabrutinib 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 Acalabrutinib guide