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 12 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. 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.
Check your bottle
Let's take a closer look at your Granisetron.
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: the form, then the strength, then the company.
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 Granisetron products leave it out.
At a glance
Which Granisetron products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseDiffers by manufacturer
3 of 12 checked products list lactose; 9 do not. See which products do not list it
-
Wheat or gluten sourceNo checked product
No checked Granisetron product lists a wheat or gluten source.
-
SoyNo checked product
No checked Granisetron product lists soy.
-
Synthetic dyesDiffers by manufacturer
1 of 12 checked products list synthetic dyes; 11 do not. See which products do not list it
-
GelatinNo checked product
No checked Granisetron product lists gelatin.
Also listed by some products: Titanium dioxide 2 of 12 Benzyl alcohol 2 of 12 PEG or polysorbate 3 of 12 Sorbitol or mannitol 1 of 12
Find a version without it
Current Granisetron products in our label sample and what each 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 size. Codes that differ only in the last part are the same product in different pack sizes and share one label, so any of them finds the right product here. Two bottles of the same medicine from different companies can have different inactive ingredients, which is why the pharmacy needs the number, not just the name.
Granisetron 1 mg/mL injection 6 companies Benzyl alcohol 2
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| EugiaNDC 55150-0175-01 | None of these listed |
Show 7 ingredientsCITRIC ACID MONOHYDRATE, HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Fresenius KabiNDC 63323-0318-01 | None of these listed |
Show 3 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM CITRATE |
| HikmaNDC 00143-9744-10 | Benzyl alcohol |
Show 6 ingredientsANHYDROUS CITRIC ACID, BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| HikmaNDC 00143-9745-05 Other pack sizes, same label: 00143-9745-10 | Benzyl alcohol |
Show 6 ingredientsANHYDROUS CITRIC ACID, BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Mylan InstitutionalNDC 67457-0863-01 | None of these listed |
Show 4 ingredientsANHYDROUS CITRIC ACID, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Mylan InstitutionalNDC 67457-0864-04 | None of these listed |
Show 4 ingredientsANHYDROUS CITRIC ACID, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE |
Granisetron 4 mg/4 mL injection 1 company none of the tracked ingredients
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| EugiaNDC 55150-0176-04 | None of these listed |
Show 7 ingredientsCITRIC ACID MONOHYDRATE, HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
Granisetron 10 mg/0.4 mL injection 1 company Polyethylene glycol or polysorbate 1
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Heron TherapeuticsNDC 47426-0101-06 | Polyethylene glycol or polysorbate |
Show 1 ingredientPOLYETHYLENE GLYCOL MONOMETHYL ETHER 550 |
Granisetron 1 mg tablet 3 companies Lactose 3 Titanium dioxide 2 Polyethylene glycol or polysorbate 2
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| BionpharmaNDC 69452-0350-01 Other pack sizes, same label: 69452-0350-11, 69452-0350-92 | Lactose |
Show 5 ingredientsCELLULOSE, MICROCRYSTALLINE, HYPROMELLOSE 2910 (3 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SODIUM STARCH GLYCOLATE TYPE A POTATO |
| BreckenridgeNDC 51991-0735-20 Other pack sizes, same label: 51991-0735-32 | 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 |
| NatcoNDC 63850-0005-01 Other pack sizes, same label: 63850-0005-02 | 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 |
Granisetron GRANISETRON 3.1 mg/24h skin patch 1 company
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| CumberlandNDC 66220-0637-31 Other pack sizes, same label: 66220-0637-72 | No inactive-ingredient list on the label | No list we could read |
Granisetron 2 mg/10 mL oral solution 1 company Synthetic dyes 1 Sorbitol or mannitol 1
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Intra-SanaNDC 80056-0801-30 | Synthetic dyes Sorbitol or mannitol |
Show 5 ingredientsANHYDROUS CITRIC ACID, FD&C YELLOW NO. 6, SODIUM BENZOATE, SORBITOL, 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.
Granisetron without lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 3 of 12 checked products list lactose; 9 do not.
Show which Granisetron products list lactose and which do not, by product and company
Does not list lactose
- 1 mg/mL injection: Eugia, Fresenius Kabi, Hikma, Hikma, Mylan Institutional, Mylan Institutional
- 4 mg/4 mL injection: Eugia
- 10 mg/0.4 mL injection: Heron Therapeutics
- 2 mg/10 mL oral solution: Intra-Sana
Lists lactose
- 1 mg tablet: Bionpharma, Breckenridge, Natco
Granisetron without synthetic dyes
Synthetic dyes: FD&C or D&C colorants and their aluminum lakes. 1 of 12 checked products list synthetic dyes; 11 do not.
Show which Granisetron products list synthetic dyes and which do not, by product and company
Does not list synthetic dyes
- 1 mg/mL injection: Eugia, Fresenius Kabi, Hikma, Hikma, Mylan Institutional, Mylan Institutional
- 4 mg/4 mL injection: Eugia
- 10 mg/0.4 mL injection: Heron Therapeutics
- 1 mg tablet: Bionpharma, Breckenridge, Natco
Lists synthetic dyes
- 2 mg/10 mL oral solution: Intra-Sana
Granisetron without titanium dioxide
Titanium dioxide: A white colorant some people choose to avoid. 2 of 12 checked products list titanium dioxide; 10 do not.
Show which Granisetron products list titanium dioxide and which do not, by product and company
Does not list titanium dioxide
- 1 mg/mL injection: Eugia, Fresenius Kabi, Hikma, Hikma, Mylan Institutional, Mylan Institutional
- 4 mg/4 mL injection: Eugia
- 10 mg/0.4 mL injection: Heron Therapeutics
- 2 mg/10 mL oral solution: Intra-Sana
- 1 mg tablet: Bionpharma
Lists titanium dioxide
- 1 mg tablet: Breckenridge, Natco
Granisetron without benzyl alcohol
Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 2 of 12 checked products list benzyl alcohol; 10 do not.
Show which Granisetron products list benzyl alcohol and which do not, by product and company
Does not list benzyl alcohol
- 1 mg/mL injection: Eugia, Fresenius Kabi, Mylan Institutional, Mylan Institutional
- 4 mg/4 mL injection: Eugia
- 10 mg/0.4 mL injection: Heron Therapeutics
- 1 mg tablet: Bionpharma, Breckenridge, Natco
- 2 mg/10 mL oral solution: Intra-Sana
Lists benzyl alcohol
- 1 mg/mL injection: Hikma, Hikma
Granisetron without polyethylene glycol or polysorbate
Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. 3 of 12 checked products list polyethylene glycol or polysorbate; 9 do not.
Show which Granisetron products list polyethylene glycol or polysorbate and which do not, by product and company
Does not list polyethylene glycol or polysorbate
- 1 mg/mL injection: Eugia, Fresenius Kabi, Hikma, Hikma, Mylan Institutional, Mylan Institutional
- 4 mg/4 mL injection: Eugia
- 2 mg/10 mL oral solution: Intra-Sana
- 1 mg tablet: Bionpharma
Lists polyethylene glycol or polysorbate
- 1 mg tablet: Breckenridge, Natco
- 10 mg/0.4 mL injection: Heron Therapeutics
Granisetron without sorbitol or mannitol
Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 1 of 12 checked products list sorbitol or mannitol; 11 do not.
Show which Granisetron products list sorbitol or mannitol and which do not, by product and company
Does not list sorbitol or mannitol
- 1 mg/mL injection: Eugia, Fresenius Kabi, Hikma, Hikma, Mylan Institutional, Mylan Institutional
- 4 mg/4 mL injection: Eugia
- 10 mg/0.4 mL injection: Heron Therapeutics
- 1 mg tablet: Bionpharma, Breckenridge, Natco
Lists sorbitol or mannitol
- 2 mg/10 mL oral solution: Intra-Sana
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?
Who decides what counts as a gluten source, a dye or soy on this page?
The NDC on my bottle ends differently from the one on this page. Is it the same product?
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