Ripretinib inactive ingredients by manufacturer
Wondering whether your Ripretinib 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 Ripretinib 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 label of 1 of the 1 current Ripretinib product 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 Ripretinib? 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 Ripretinib products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseEvery checked product
Every checked Ripretinib product (1) lists lactose. See the products
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Wheat or gluten sourceNo checked product
No checked Ripretinib product lists a wheat or gluten source.
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SoyNo checked product
No checked Ripretinib product lists soy.
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Synthetic dyesNo checked product
No checked Ripretinib product lists synthetic dyes.
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GelatinNo checked product
No checked Ripretinib product lists gelatin.
Find a version without it
Every current Ripretinib product and what its label lists
Ripretinib 50 mg tablet 1 company Lactose 1
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| DecipheraNDC 73207-0101-30 | Lactose |
Show 6 ingredientscrospovidone, hypromellose acetate succinate 06081224 (3 MM2/S), lactose monohydrate, magnesium stearate, microcrystalline cellulose, silicon dioxide |
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.
Ripretinib and lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. Every checked Ripretinib product (1) lists lactose.
Show which Ripretinib products list lactose and which do not, by product and company
Lists lactose
- 50 mg tablet: Deciphera
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 Ripretinib inactive ingredients
Is Ripretinib gluten-free?
Does Ripretinib contain lactose?
Does Ripretinib contain soy?
Is there a dye-free Ripretinib?
Does Ripretinib 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 Ripretinib 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 Ripretinib guide