Granisetron inactive ingredients by manufacturer
Wondering whether your Granisetron 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 Granisetron 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 8 of the 13 current Granisetron products on the market today, from 10 companies listing it with the FDA, and lined them up side by side. The FDA directory lists 14 current products in all; this page covers the 13 we hold labels for. 4 are still being read and will appear on a later visit. 1 label has no inactive-ingredient list we could read, so that product cannot be compared.
Ask about your bottle
Is there something in your Granisetron? 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 Granisetron products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseDiffers by manufacturer
3 of 8 checked products list lactose; 5 do not. See the products
-
Wheat or gluten sourceNo checked product
No checked Granisetron product lists a wheat or gluten source.
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SoyNo checked product
No checked Granisetron product lists soy.
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Synthetic dyesDiffers by manufacturer
1 of 8 checked products list synthetic dyes; 7 do not. See the products
Lists it Intra-Sana -
GelatinNo checked product
No checked Granisetron product lists gelatin.
Also listed by some products: Titanium dioxide 2 of 8 PEG or polysorbate 3 of 8 Sorbitol or mannitol 1 of 8
Find a version without it
Current Granisetron products in our label sample and what each label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Bionpharma Inc. 1 product | ||
| 1 mg tabletNDC 69452-0350-01 | Lactose |
Show 5 ingredientsCELLULOSE, MICROCRYSTALLINE, HYPROMELLOSE 2910 (3 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SODIUM STARCH GLYCOLATE TYPE A POTATO |
| Breckenridge Pharmaceutical, Inc. 1 product | ||
| 1 mg tabletNDC 51991-0735-20 | Lactose Titanium dioxide Polyethylene glycol or polysorbate |
Show 8 ingredientsHYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 4000, POLYSORBATE 80, SODIUM STARCH GLYCOLATE TYPE A POTATO, TITANIUM DIOXIDE |
| Cumberland Pharmaceuticals Inc. 1 product | ||
| GRANISETRON 3.1 mg/24h skin patchNDC 66220-0637-31 | No inactive-ingredient list on the label | No list we could read |
| Eugia US LLC 2 products | ||
| 1 mg/mL injectionNDC 55150-0175-01 | None of these listed |
Show 7 ingredientsCITRIC ACID MONOHYDRATE, HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 4 mg/4 mL injectionNDC 55150-0176-04 | None of these listed |
Show 7 ingredientsCITRIC ACID MONOHYDRATE, HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Fresenius Kabi USA, LLC 1 product | ||
| 1 mg/mL injectionNDC 63323-0318-01 | None of these listed |
Show 3 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM CITRATE |
| Heron Therapeutics, Inc. 1 product | ||
| 10 mg/0.4 mL injectionNDC 47426-0101-06 | Polyethylene glycol or polysorbate |
Show 1 ingredientPOLYETHYLENE GLYCOL MONOMETHYL ETHER 550 |
| Hikma Pharmaceuticals USA Inc. 2 products | ||
| 1 mg/mL injectionNDC 00143-9744-10 | Still being read | Not read yet |
| 1 mg/mL injectionNDC 00143-9745-05 | Still being read | Not read yet |
| Intra-Sana Laboratories 1 product | ||
| 2 mg/10 mL oral solutionNDC 80056-0801-30 | Synthetic dyes Sorbitol or mannitol |
Show 5 ingredientsANHYDROUS CITRIC ACID, FD&C YELLOW NO. 6, SODIUM BENZOATE, SORBITOL, WATER |
| Mylan Institutional LLC 2 products | ||
| 1 mg/mL injectionNDC 67457-0863-01 | Still being read | Not read yet |
| 1 mg/mL injectionNDC 67457-0864-04 | Still being read | Not read yet |
| Natco Pharma Limited 1 product | ||
| 1 mg tabletNDC 63850-0005-01 | Lactose Titanium dioxide Polyethylene glycol or polysorbate |
Show 8 ingredientsCELLULOSE, MICROCRYSTALLINE, HYPROMELLOSES, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYSORBATE 80, SODIUM STARCH GLYCOLATE TYPE A POTATO, 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.
Granisetron without lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 3 of 8 checked products list lactose; 5 do not.
Does not list lactose
- Eugia: 1 mg/mL injection, 4 mg/4 mL injection
- Fresenius Kabi: 1 mg/mL injection
- Heron Therapeutics: 10 mg/0.4 mL injection
- Intra-Sana: 2 mg/10 mL oral solution
Lists lactose
- Bionpharma: 1 mg tablet
- Breckenridge: 1 mg tablet
- Natco: 1 mg tablet
Granisetron without synthetic dyes
Synthetic dyes: FD&C or D&C colorants and their aluminum lakes. 1 of 8 checked products list synthetic dyes; 7 do not.
Does not list synthetic dyes
- Bionpharma: 1 mg tablet
- Breckenridge: 1 mg tablet
- Eugia: 1 mg/mL injection, 4 mg/4 mL injection
- Fresenius Kabi: 1 mg/mL injection
- Heron Therapeutics: 10 mg/0.4 mL injection
- Natco: 1 mg tablet
Lists synthetic dyes
- Intra-Sana: 2 mg/10 mL oral solution
Granisetron without titanium dioxide
Titanium dioxide: A white colorant some people choose to avoid. 2 of 8 checked products list titanium dioxide; 6 do not.
Does not list titanium dioxide
- Bionpharma: 1 mg tablet
- Eugia: 1 mg/mL injection, 4 mg/4 mL injection
- Fresenius Kabi: 1 mg/mL injection
- Heron Therapeutics: 10 mg/0.4 mL injection
- Intra-Sana: 2 mg/10 mL oral solution
Lists titanium dioxide
- Breckenridge: 1 mg tablet
- Natco: 1 mg tablet
Granisetron without polyethylene glycol or polysorbate
Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. 3 of 8 checked products list polyethylene glycol or polysorbate; 5 do not.
Does not list polyethylene glycol or polysorbate
- Bionpharma: 1 mg tablet
- Eugia: 1 mg/mL injection, 4 mg/4 mL injection
- Fresenius Kabi: 1 mg/mL injection
- Intra-Sana: 2 mg/10 mL oral solution
Lists polyethylene glycol or polysorbate
- Breckenridge: 1 mg tablet
- Heron Therapeutics: 10 mg/0.4 mL injection
- Natco: 1 mg tablet
Granisetron without sorbitol or mannitol
Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 1 of 8 checked products list sorbitol or mannitol; 7 do not.
Does not list sorbitol or mannitol
- Bionpharma: 1 mg tablet
- Breckenridge: 1 mg tablet
- Eugia: 1 mg/mL injection, 4 mg/4 mL injection
- Fresenius Kabi: 1 mg/mL injection
- Heron Therapeutics: 10 mg/0.4 mL injection
- Natco: 1 mg tablet
Lists sorbitol or mannitol
- Intra-Sana: 2 mg/10 mL oral solution
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 Granisetron inactive ingredients
Is Granisetron gluten-free?
Does Granisetron contain lactose?
Does Granisetron contain soy?
Is there a dye-free Granisetron?
Does Granisetron 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 Granisetron 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 Granisetron guide