Paclitaxel inactive ingredients by manufacturer
Wondering whether your Paclitaxel 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 Paclitaxel 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 30 of the 40 current Paclitaxel products on the market today, from 22 companies listing it with the FDA, and lined them up side by side. The FDA directory lists 41 current products in all; this page covers the 40 we hold labels for. 10 are still being read and will appear on a later visit.
Ask about your bottle
Is there something in your Paclitaxel? 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 Paclitaxel products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Paclitaxel product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Paclitaxel product lists a wheat or gluten source.
-
SoyNo checked product
No checked Paclitaxel product lists soy.
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Synthetic dyesNo checked product
No checked Paclitaxel product lists synthetic dyes.
-
GelatinNo checked product
No checked Paclitaxel product lists gelatin.
Also listed by some products: Alcohol 19 of 30
Find a version without it
Current Paclitaxel products in our label sample and what each label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Abraxis BioScience, LLC 1 product | ||
| 100 mg/20 mL injectionNDC 68817-0134-50 | None of these listed |
Show 1 ingredientALBUMIN HUMAN |
| Alembic Pharmaceuticals Inc. 3 products | ||
| 6 mg/mL injectionNDC 62332-0622-50 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 62332-0621-17 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 62332-0620-05 | Still being read | Not read yet |
| Alembic Pharmaceuticals Limited 3 products | ||
| 6 mg/mL injectionNDC 46708-0622-50 | Still being read | Not read yet |
| 6 mg/mL injectionNDC 46708-0621-17 | Still being read | Not read yet |
| 6 mg/mL injectionNDC 46708-0620-05 | Still being read | Not read yet |
| American Regent, Inc. 1 product | ||
| 100 mg/20 mL injectionNDC 00517-4300-01 | Still being read | Not read yet |
| BluePoint Laboratories 3 products | ||
| 6 mg/mL injectionNDC 68001-0705-27 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 68001-0516-27 | None of these listed |
Show 3 ingredientsCASTOR OIL, CITRIC ACID MONOHYDRATE, POLYOXYL 35 CASTOR OIL |
| 100 mg/20 mL injectionNDC 68001-0651-37 | None of these listed |
Show 1 ingredientALBUMIN HUMAN |
| Bryant Ranch Prepack 1 product | ||
| 6 mg/mL injectionNDC 72162-2640-02 | None of these listed |
Show 3 ingredientsCASTOR OIL, CITRIC ACID MONOHYDRATE, POLYOXYL 35 CASTOR OIL |
| Cipla USA Inc. 1 product | ||
| 100 mg/20 mL injectionNDC 69097-0398-78 | None of these listed |
Show 1 ingredientALBUMIN HUMAN |
| Exelan Pharmaceuticals Inc. 1 product | ||
| 100 mg/20 mL injectionNDC 76282-0768-09 | None of these listed |
Show 1 ingredientALBUMIN HUMAN |
| Fresenius Kabi USA, LLC 1 product | ||
| 6 mg/mL injectionNDC 63323-0763-05 | Alcohol (ethanol) |
Show 2 ingredientsALCOHOL, POLYOXYL 35 CASTOR OIL |
| Gland Pharma Limited 3 products | ||
| 6 mg/mL injectionNDC 68083-0180-01 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 68083-0178-01 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 68083-0179-01 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 3 products | ||
| 6 mg/mL injectionNDC 23155-0884-31 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 23155-0882-31 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 23155-0883-31 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| Hospira, Inc. 2 products | ||
| 6 mg/mL injectionNDC 61703-0342-09 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, CITRIC ACID MONOHYDRATE, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 61703-0015-04 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, CITRIC ACID MONOHYDRATE, POLYOXYL 35 CASTOR OIL |
| Meitheal Pharmaceuticals Inc. 1 product | ||
| 100 mg/20 mL injectionNDC 71288-0183-50 | Still being read | Not read yet |
| Mylan Institutional LLC 1 product | ||
| 100 mg/20 mL injectionNDC 67457-0937-50 | Still being read | Not read yet |
| Natco Pharma USA LLC 3 products | ||
| 6 mg/mL injectionNDC 69339-0227-05 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 69339-0228-17 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 69339-0229-50 | Still being read | Not read yet |
| Northstar Rx LLC 1 product | ||
| 6 mg/mL injectionNDC 16714-0137-01 | None of these listed |
Show 3 ingredientsCASTOR OIL, CITRIC ACID MONOHYDRATE, POLYOXYL 35 CASTOR OIL |
| NorthStar Rx LLC 1 product | ||
| 100 mg/20 mL injectionNDC 72603-0408-01 | Still being read | Not read yet |
| Novadoz Pharmaceuticals LLC 3 products | ||
| 6 mg/mL injectionNDC 72205-0061-01 | Still being read | Not read yet |
| 6 mg/mL injectionNDC 72205-0063-01 | None of these listed |
Show 3 ingredientsCASTOR OIL, CITRIC ACID MONOHYDRATE, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 72205-0062-01 | None of these listed |
Show 3 ingredientsCASTOR OIL, CITRIC ACID MONOHYDRATE, POLYOXYL 35 CASTOR OIL |
| Sagent Pharmaceuticals 1 product | ||
| 6 mg/mL injectionNDC 25021-0255-05 | Alcohol (ethanol) |
Show 3 ingredientsAlcohol, Anhydrous Citric Acid, Polyoxyl 35 Castor Oil |
| Sandoz Inc 1 product | ||
| 100 mg/20 mL injectionNDC 00781-3531-91 | None of these listed |
Show 1 ingredientALBUMIN HUMAN |
| Teva Pharmaceuticals, Inc. 1 product | ||
| 100 mg/20 mL injectionNDC 00480-3290-01 | None of these listed |
Show 2 ingredientsALBUMIN HUMAN, SODIUM CHLORIDE |
| Teva Parenteral Medicines, Inc. 4 products | ||
| 6 mg/mL injectionNDC 00703-3213-01 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 00703-3216-01 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 00703-3218-01 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
| 6 mg/mL injectionNDC 00703-3217-01 | Alcohol (ethanol) |
Show 3 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, POLYOXYL 35 CASTOR OIL |
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.
Paclitaxel without alcohol (ethanol)
Alcohol (ethanol): mostly in liquids; a concern in alcohol recovery, for children, or with disulfiram or metronidazole. 19 of 30 checked products list alcohol (ethanol); 11 do not.
Does not list alcohol (ethanol)
- Abraxis BioScience: 100 mg/20 mL injection
- BluePoint: 6 mg/mL injection, 100 mg/20 mL injection
- Bryant Ranch Prepack: 6 mg/mL injection
- Cipla: 100 mg/20 mL injection
- Exelan: 100 mg/20 mL injection
- Northstar Rx: 6 mg/mL injection
- Novadoz: 6 mg/mL injection (NDC 72205-0063-01), 6 mg/mL injection (NDC 72205-0062-01)
- Sandoz: 100 mg/20 mL injection
- Teva: 100 mg/20 mL injection
Lists alcohol (ethanol)
- Alembic Pharmaceuticals Inc.: 6 mg/mL injection (NDC 62332-0622-50), 6 mg/mL injection (NDC 62332-0621-17)
- BluePoint: 6 mg/mL injection
- Fresenius Kabi: 6 mg/mL injection
- Gland: 6 mg/mL injection (NDC 68083-0180-01), 6 mg/mL injection (NDC 68083-0178-01), 6 mg/mL injection (NDC 68083-0179-01)
- Heritage Pharmaceuticals Inc. d/b/a Avet: 6 mg/mL injection (NDC 23155-0884-31), 6 mg/mL injection (NDC 23155-0882-31), 6 mg/mL injection (NDC 23155-0883-31)
- Hospira: 6 mg/mL injection (NDC 61703-0342-09), 6 mg/mL injection (NDC 61703-0015-04)
- Natco: 6 mg/mL injection (NDC 69339-0227-05), 6 mg/mL injection (NDC 69339-0228-17)
- Sagent: 6 mg/mL injection
- Teva Parenteral Medicines: 6 mg/mL injection (NDC 00703-3213-01), 6 mg/mL injection (NDC 00703-3216-01), 6 mg/mL injection (NDC 00703-3218-01), 6 mg/mL injection (NDC 00703-3217-01)
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 Paclitaxel inactive ingredients
Is Paclitaxel gluten-free?
Does Paclitaxel contain lactose?
Does Paclitaxel contain soy?
Is there a dye-free Paclitaxel?
Does Paclitaxel 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 Paclitaxel 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 Paclitaxel guide