Oxaliplatin Injection inactive ingredients by manufacturer
Wondering whether your Oxaliplatin 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 Oxaliplatin 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 40 of the 40 current Oxaliplatin Injection products on the market today, from 17 companies listing it with the FDA, and lined them up side by side.
Ask about your bottle
Is there something in your Oxaliplatin 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 Oxaliplatin Injection products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseDiffers by manufacturer
4 of 40 checked products list lactose; 36 do not. See the products
-
Wheat or gluten sourceNo checked product
No checked Oxaliplatin Injection product lists a wheat or gluten source.
-
SoyNo checked product
No checked Oxaliplatin Injection product lists soy.
-
Synthetic dyesNo checked product
No checked Oxaliplatin Injection product lists synthetic dyes.
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GelatinNo checked product
No checked Oxaliplatin Injection product lists gelatin.
Find a version without it
Every current Oxaliplatin Injection product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Accord Healthcare Inc. 1 product | ||
| 5 mg/mL injectionNDC 16729-0332-03 | None of these listed |
Show 1 ingredientWATER |
| Apotex Corp. 2 products | ||
| 5 mg/mL injectionNDC 60505-6132-06 | None of these listed |
Show 1 ingredientwater |
| 5 mg/mL injectionNDC 60505-6287-02 | None of these listed |
Show 1 ingredientwater |
| Baxter Healthcare Corporation 2 products | ||
| 5 mg/mL injectionNDC 43066-0018-01 | None of these listed |
Show 1 ingredientWATER |
| 5 mg/mL injectionNDC 43066-0014-01 | None of these listed |
Show 1 ingredientWATER |
| BluePoint Laboratories 1 product | ||
| 5 mg/mL injectionNDC 68001-0468-36 | None of these listed |
Show 1 ingredientWATER |
| Camber Pharmaceuticals, Inc. 2 products | ||
| 50 mg/10 mL injectionNDC 31722-0357-10 | None of these listed |
Show 1 ingredientWATER |
| 100 mg/20 mL injectionNDC 31722-0358-20 | None of these listed |
Show 1 ingredientWATER |
| Eugia US LLC 2 products | ||
| 5 mg/mL injectionNDC 55150-0332-01 | None of these listed |
Show 1 ingredientWATER |
| 5 mg/mL injectionNDC 55150-0331-01 | None of these listed |
Show 1 ingredientWATER |
| Fosun Pharma Usa Inc. 2 products | ||
| 5 mg/mL injectionNDC 72266-0162-01 | None of these listed |
Show 1 ingredientWATER |
| 5 mg/mL injectionNDC 72266-0161-01 | None of these listed |
Show 1 ingredientWATER |
| Gland Pharma Limited 5 products | ||
| 5 mg/mL injectionNDC 68083-0177-01 | None of these listed |
Show 1 ingredientWATER |
| 5 mg/mL injectionNDC 68083-0176-01 | None of these listed |
Show 1 ingredientWATER |
| 5 mg/mL injectionNDC 68083-0314-01 | None of these listed |
Show 1 ingredientWATER |
| 50 mg/10 mL injectionNDC 68083-0170-01 | Lactose |
Show 1 ingredientLACTOSE MONOHYDRATE |
| 100 mg/20 mL injectionNDC 68083-0171-01 | Lactose |
Show 1 ingredientLACTOSE MONOHYDRATE |
| Hospira, Inc. 1 product | ||
| 5 mg/mL injectionNDC 61703-0363-18 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, TARTARIC ACID, WATER |
| Meitheal Pharmaceuticals Inc. 4 products | ||
| 5 mg/mL injectionNDC 71288-0171-11 | None of these listed |
Show 1 ingredientwater |
| 5 mg/mL injectionNDC 71288-0172-21 | None of these listed |
Show 1 ingredientwater |
| 5 mg/mL injectionNDC 71288-0101-10 | None of these listed |
Show 1 ingredientwater |
| 5 mg/mL injectionNDC 71288-0149-95 | None of these listed |
Show 1 ingredientwater |
| Mylan Institutional LLC 2 products | ||
| 5 mg/mL injectionNDC 67457-0469-10 | None of these listed |
Show 1 ingredientWATER |
| 5 mg/mL injectionNDC 67457-0442-20 | None of these listed |
Show 1 ingredientWATER |
| NorthStar Rx LLC 2 products | ||
| 5 mg/mL injectionNDC 72603-0101-01 | None of these listed |
Show 1 ingredientwater |
| 5 mg/mL injectionNDC 72603-0301-01 | None of these listed |
Show 1 ingredientwater |
| Northstar Rx LLC 2 products | ||
| 5 mg/mL injectionNDC 72603-0320-01 | None of these listed |
Show 1 ingredientwater |
| 5 mg/mL injectionNDC 72603-0420-01 | None of these listed |
Show 1 ingredientwater |
| Qilu Pharmaceutical Co., Ltd. 5 products | ||
| 50 mg/10 mL injectionNDC 67184-0501-01 | Lactose |
Show 1 ingredientLACTOSE MONOHYDRATE |
| 50 mg/10 mL injectionNDC 67184-0508-01 | None of these listed |
Show 1 ingredientWater |
| 100 mg/20 mL injectionNDC 67184-0502-01 | Lactose |
Show 1 ingredientLACTOSE MONOHYDRATE |
| 100 mg/20 mL injectionNDC 67184-0509-01 | None of these listed |
Show 1 ingredientWater |
| 200 mg/40 mL injectionNDC 67184-0510-01 | None of these listed |
Show 1 ingredientwater |
| Sagent Pharmaceuticals 1 product | ||
| 5 mg/mL injectionNDC 25021-0233-10 | None of these listed |
Show 3 ingredientssodium hydroxide, tartaric acid, water |
| Sandoz Inc 4 products | ||
| 5 mg/mL injectionNDC 00781-9315-70 | None of these listed |
Show 1 ingredientWATER |
| 5 mg/mL injectionNDC 00781-9317-80 | None of these listed |
Show 1 ingredientWATER |
| 5 mg/mL injectionNDC 00781-3317-80 | None of these listed |
Show 1 ingredientWATER |
| 5 mg/mL injectionNDC 00781-3315-70 | None of these listed |
Show 1 ingredientWATER |
| Shandong New Time Pharmaceutical Co., Ltd. 2 products | ||
| 5 mg/mL injectionNDC 42677-0336-10 | None of these listed |
Show 1 ingredientWATER |
| 5 mg/mL injectionNDC 42677-0337-10 | None of these listed |
Show 1 ingredientWATER |
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.
Oxaliplatin Injection without lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 4 of 40 checked products list lactose; 36 do not.
Does not list lactose
- Accord Healthcare: 5 mg/mL injection
- Apotex: 5 mg/mL injection (NDC 60505-6132-06), 5 mg/mL injection (NDC 60505-6287-02)
- Baxter Healthcare: 5 mg/mL injection (NDC 43066-0018-01), 5 mg/mL injection (NDC 43066-0014-01)
- BluePoint: 5 mg/mL injection
- Camber: 50 mg/10 mL injection, 100 mg/20 mL injection
- Eugia: 5 mg/mL injection (NDC 55150-0332-01), 5 mg/mL injection (NDC 55150-0331-01)
- Fosun: 5 mg/mL injection (NDC 72266-0162-01), 5 mg/mL injection (NDC 72266-0161-01)
- Gland: 5 mg/mL injection (NDC 68083-0177-01), 5 mg/mL injection (NDC 68083-0176-01), 5 mg/mL injection (NDC 68083-0314-01)
- Hospira: 5 mg/mL injection
- Meitheal: 5 mg/mL injection (NDC 71288-0171-11), 5 mg/mL injection (NDC 71288-0172-21), 5 mg/mL injection (NDC 71288-0101-10), 5 mg/mL injection (NDC 71288-0149-95)
- Mylan Institutional: 5 mg/mL injection (NDC 67457-0469-10), 5 mg/mL injection (NDC 67457-0442-20)
- NorthStar Rx: 5 mg/mL injection (NDC 72603-0101-01), 5 mg/mL injection (NDC 72603-0301-01)
- Northstar Rx: 5 mg/mL injection (NDC 72603-0320-01), 5 mg/mL injection (NDC 72603-0420-01)
- Qilu: 50 mg/10 mL injection, 100 mg/20 mL injection, 200 mg/40 mL injection
- Sagent: 5 mg/mL injection
- Sandoz: 5 mg/mL injection (NDC 00781-9315-70), 5 mg/mL injection (NDC 00781-9317-80), 5 mg/mL injection (NDC 00781-3317-80), 5 mg/mL injection (NDC 00781-3315-70)
- Shandong New Time: 5 mg/mL injection (NDC 42677-0336-10), 5 mg/mL injection (NDC 42677-0337-10)
Lists lactose
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 Oxaliplatin Injection inactive ingredients
Is Oxaliplatin Injection gluten-free?
Does Oxaliplatin Injection contain lactose?
Does Oxaliplatin Injection contain soy?
Is there a dye-free Oxaliplatin Injection?
Does Oxaliplatin 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 Oxaliplatin Injection 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 Oxaliplatin Injection guide