Palonosetron Injection inactive ingredients by manufacturer
Wondering whether your Palonosetron Injection 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 Palonosetron Injection 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 18 of the 18 current Palonosetron Injection products on the market today, from 16 companies listing it with the FDA, and lined them up side by side.
Ask about your bottle
Is there something in your Palonosetron Injection? 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 Palonosetron Injection products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Palonosetron Injection product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Palonosetron Injection product lists a wheat or gluten source.
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SoyNo checked product
No checked Palonosetron Injection product lists soy.
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Synthetic dyesNo checked product
No checked Palonosetron Injection product lists synthetic dyes.
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GelatinNo checked product
No checked Palonosetron Injection product lists gelatin.
Also listed by some products: Sorbitol or mannitol 18 of 18
Find a version without it
Every current Palonosetron Injection product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Apotex Corp. 2 products | ||
| 0.25 mg/5 mL injectionNDC 60505-6439-01 | Sorbitol or mannitol |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, MANNITOL, SODIUM CITRATE, WATER |
| 0.25 mg/5 mL injectionNDC 60505-6193-01 | Sorbitol or mannitol |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, MANNITOL, SODIUM CITRATE, WATER |
| Avyxa Pharma, LLC 1 product | ||
| 0.25 mg/5 mL injectionNDC 83831-0105-01 | Sorbitol or mannitol |
Show 3 ingredientsMANNITOL, SODIUM ACETATE, WATER |
| Baxter Healthcare Corporation 1 product | ||
| 0.25 mg/5 mL injectionNDC 36000-0326-02 | Sorbitol or mannitol |
Show 5 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, MANNITOL, SODIUM CITRATE, UNSPECIFIED FORM, WATER |
| BluePoint Laboratories 1 product | ||
| 0.05 mg/mL injectionNDC 68001-0355-25 | Sorbitol or mannitol |
Show 4 ingredientsEDETATE DISODIUM, MANNITOL, SODIUM ACETATE, WATER |
| BLuePoint Laboratories 1 product | ||
| 0.25 mg/5 mL injectionNDC 68001-0708-25 | Sorbitol or mannitol |
Show 3 ingredientsCITRIC ACID MONOHYDRATE, MANNITOL, SODIUM CITRATE, UNSPECIFIED FORM |
| Cipla USA Inc. 1 product | ||
| 0.25 mg/5 mL injectionNDC 69097-0927-35 | Sorbitol or mannitol |
Show 5 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, MANNITOL, SODIUM CITRATE, WATER |
| Dr.Reddy's Laboratories Limited 1 product | ||
| 0.05 mg/mL injectionNDC 55111-0694-07 | Sorbitol or mannitol |
Show 4 ingredientsedetate disodium, mannitol, sodium acetate, water |
| Eugia US LLC 1 product | ||
| 0.25 mg/5 mL injectionNDC 55150-0186-05 | Sorbitol or mannitol |
Show 7 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| Fresenius Kabi USA, LLC 1 product | ||
| 0.25 mg/5 mL injectionNDC 63323-0673-05 | Sorbitol or mannitol |
Show 6 ingredientsanhydrous citric acid, edetate disodium, Hydrochloric Acid, Mannitol, Sodium Hydroxide, trisodium citrate dihydrate |
| Meitheal Pharmaceuticals Inc. 1 product | ||
| 0.25 mg/5 mL injectionNDC 71288-0409-05 | Sorbitol or mannitol |
Show 7 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| Mylan Institutional LLC 1 product | ||
| 0.25 mg/5 mL injectionNDC 67457-0317-25 | Sorbitol or mannitol |
Show 7 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, MANNITOL, SODIUM CITRATE, UNSPECIFIED FORM, SODIUM HYDROXIDE, WATER |
| NorthStar Rx LLC 1 product | ||
| 0.05 mg/mL injectionNDC 16714-0834-01 | Sorbitol or mannitol |
Show 4 ingredientsedetate disodium, mannitol, sodium acetate, water |
| Qilu Pharmaceutical Co., Ltd. 2 products | ||
| 0.075 mg/1.5 mL injectionNDC 67184-0515-02 | Sorbitol or mannitol |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, MANNITOL, SODIUM CITRATE, WATER |
| 0.25 mg/5 mL injectionNDC 67184-0514-01 | Sorbitol or mannitol |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, MANNITOL, SODIUM CITRATE, WATER |
| Sagent Pharmaceuticals 1 product | ||
| 0.05 mg/mL injectionNDC 25021-0783-05 | Sorbitol or mannitol |
Show 7 ingredientscitric acid monohydrate, edetate disodium, hydrochloric acid, mannitol, sodium hydroxide, Trisodium Citrate Dihydrate, water |
| Sandoz Inc 1 product | ||
| 0.25 mg/5 mL injectionNDC 00781-3312-75 | Sorbitol or mannitol |
Show 7 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| Teva Parenteral Medicines, Inc. 1 product | ||
| 0.25 mg/5 mL injectionNDC 00703-4094-01 | Sorbitol or mannitol |
Show 7 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE, TRISODIUM CITRATE DIHYDRATE, 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.
Palonosetron Injection and sorbitol or mannitol
Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. Every checked Palonosetron Injection product (18) lists sorbitol or mannitol.
Lists sorbitol or mannitol
- Apotex: 0.25 mg/5 mL injection (NDC 60505-6439-01), 0.25 mg/5 mL injection (NDC 60505-6193-01)
- Avyxa: 0.25 mg/5 mL injection
- Baxter Healthcare: 0.25 mg/5 mL injection
- BluePoint: 0.05 mg/mL injection
- BLuePoint: 0.25 mg/5 mL injection
- Cipla: 0.25 mg/5 mL injection
- Dr.Reddy's: 0.05 mg/mL injection
- Eugia: 0.25 mg/5 mL injection
- Fresenius Kabi: 0.25 mg/5 mL injection
- Meitheal: 0.25 mg/5 mL injection
- Mylan Institutional: 0.25 mg/5 mL injection
- NorthStar Rx: 0.05 mg/mL injection
- Qilu: 0.075 mg/1.5 mL injection, 0.25 mg/5 mL injection
- Sagent: 0.05 mg/mL injection
- Sandoz: 0.25 mg/5 mL injection
- Teva Parenteral Medicines: 0.25 mg/5 mL injection
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 Palonosetron Injection inactive ingredients
Is Palonosetron Injection gluten-free?
Does Palonosetron Injection contain lactose?
Does Palonosetron Injection contain soy?
Is there a dye-free Palonosetron Injection?
Does Palonosetron Injection 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 Palonosetron Injection products in the FDA's current NDC directory (openFDA), as of October 5, 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 Palonosetron Injection guide