Erdafitinib inactive ingredients by manufacturer
Wondering whether your Erdafitinib 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 Erdafitinib 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 Erdafitinib 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 Erdafitinib? 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.
Check your bottle
Let's take a closer look at your Erdafitinib.
Pick your bottle and tap what you want to check. The answer comes from that product's own FDA label, which is already on this page.
1 Which bottle do you have?
Or tap your way to it, one step at a time:
2 What do you want to check?
Nothing tapped? We check the five big ones.
Pick your bottle to read its label, or tap an ingredient to see which Erdafitinib products leave it out.
At a glance
Which Erdafitinib products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Erdafitinib product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Erdafitinib product lists a wheat or gluten source.
-
SoyNo checked product
No checked Erdafitinib product lists soy.
-
Synthetic dyesNo checked product
No checked Erdafitinib product lists synthetic dyes.
-
GelatinNo checked product
No checked Erdafitinib product lists gelatin.
Also listed by some products: Titanium dioxide 3 of 3 Sorbitol or mannitol 3 of 3
Find a version without it
Every current Erdafitinib product and what its label lists
Fastest way: search by NDC. It is printed on your bottle's pharmacy label. If it is not, call your pharmacy: they have it on record.
An NDC (National Drug Code) is the FDA's number for one exact product from one company in one package size, written like 60505-0121-01: the first part is the company, the middle the product and strength, the last the package. Two bottles of the same medicine with different NDCs can have different inactive ingredients, which is why the pharmacy needs the number, not just the name.
Erdafitinib 3 mg tablet 1 company Titanium dioxide 1 Sorbitol or mannitol 1
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Janssen ProductsNDC 59676-0030-56 | Titanium dioxide Sorbitol or mannitol |
Show 11 ingredientsCROSCARMELLOSE SODIUM, FERRIC OXIDE YELLOW, GLYCERYL MONOCAPRYLOCAPRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, MICROCRYSTALLINE CELLULOSE, POLYVINYL ALCOHOL, UNSPECIFIED, SODIUM LAURYL SULFATE, TALC, TITANIUM DIOXIDE |
Erdafitinib 4 mg tablet 1 company Titanium dioxide 1 Sorbitol or mannitol 1
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Janssen ProductsNDC 59676-0040-28 | Titanium dioxide Sorbitol or mannitol |
Show 12 ingredientsCROSCARMELLOSE SODIUM, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, GLYCERYL MONOCAPRYLOCAPRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, MICROCRYSTALLINE CELLULOSE, POLYVINYL ALCOHOL, UNSPECIFIED, SODIUM LAURYL SULFATE, TALC, TITANIUM DIOXIDE |
Erdafitinib 5 mg tablet 1 company Titanium dioxide 1 Sorbitol or mannitol 1
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Janssen ProductsNDC 59676-0050-28 | Titanium dioxide Sorbitol or mannitol |
Show 13 ingredientsCROSCARMELLOSE SODIUM, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, FERROSOFERRIC OXIDE, GLYCERYL MONOCAPRYLOCAPRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, MICROCRYSTALLINE CELLULOSE, POLYVINYL ALCOHOL, UNSPECIFIED, SODIUM LAURYL SULFATE, TALC, TITANIUM 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.
Erdafitinib and titanium dioxide
Titanium dioxide: A white colorant some people choose to avoid. Every checked Erdafitinib product (3) lists titanium dioxide.
Show which Erdafitinib products list titanium dioxide and which do not, by product and company
Lists titanium dioxide
- 3 mg tablet: Janssen Products
- 4 mg tablet: Janssen Products
- 5 mg tablet: Janssen Products
Erdafitinib and sorbitol or mannitol
Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. Every checked Erdafitinib product (3) lists sorbitol or mannitol.
Show which Erdafitinib products list sorbitol or mannitol and which do not, by product and company
Lists sorbitol or mannitol
- 3 mg tablet: Janssen Products
- 4 mg tablet: Janssen Products
- 5 mg tablet: Janssen Products
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 Erdafitinib inactive ingredients
Is Erdafitinib gluten-free?
Does Erdafitinib contain lactose?
Does Erdafitinib contain soy?
Is there a dye-free Erdafitinib?
Does Erdafitinib contain gelatin?
Why do the inactive ingredients differ between manufacturers?
Who decides what counts as a gluten source, a dye or soy on this page?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Erdafitinib 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 Erdafitinib guide