Inactive ingredients by manufacturer

Bortezomib inactive ingredients by manufacturer

Wondering whether your Bortezomib 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 Bortezomib 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 24 of the 31 current Bortezomib products on the market today, from 25 companies listing it with the FDA, and lined them up side by side. The FDA directory lists 32 current products in all; this page covers the 31 we hold labels for. 5 are still being read and will appear on a later visit. 2 labels have no inactive-ingredient list we could read, so those products cannot be compared.

Ask about your bottle

Is there something in your Bortezomib? 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 Bortezomib products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseNo checked product

    No checked Bortezomib product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Bortezomib product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Bortezomib product lists soy.

  4. Synthetic dyesNo checked product

    No checked Bortezomib product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Bortezomib product lists gelatin.

Also listed by some products: Sorbitol or mannitol 24 of 24

Find a version without it

Current Bortezomib products in our label sample and what each label lists

Hide products that list:

ProductListsInactive ingredients on the label
Amneal Pharmaceuticals LLC 1 product
3.5 mg/1.4 mL injectionNDC 70121-2484-01 No inactive-ingredient list on the label No list we could read
Apotex Corp 1 product
3.5 mg injectionNDC 60505-6050-04 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
Avenacy, LLC 1 product
3.5 mg injectionNDC 83634-0208-10 Sorbitol or mannitol
Show 1 ingredient

mannitol
BluePoint Laboratories 3 products
3.5 mg injectionNDC 68001-0534-36 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
3.5 mg injectionNDC 68001-0540-36 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
3.5 mg/3.5 mL injectionNDC 68001-0541-36 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
Camber Pharmaceuticals, Inc. 1 product
3.5 mg injectionNDC 31722-0303-31 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
Dr.Reddy's Laboratories, Inc. 1 product
3.5 mg injectionNDC 43598-0426-60 Sorbitol or mannitol
Show 1 ingredient

mannitol
Eugia US LLC 1 product
3.5 mg injectionNDC 55150-0337-01 Still being read Not read yet
Fresenius Kabi USA, LLC 1 product
3.5 mg injectionNDC 63323-0821-10 Sorbitol or mannitol
Show 1 ingredient

Mannitol
Gland Pharma Limited 2 products
1 mg injectionNDC 68083-0650-01 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
2.5 mg injectionNDC 68083-0651-01 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
Hikma Pharmaceuticals USA Inc. 1 product
3.5 mg injectionNDC 00143-9098-01 Sorbitol or mannitol
Show 1 ingredient

mannitol
Hospira, Inc. 3 products
1 mg injectionNDC 00409-1704-01 Still being read Not read yet
2.5 mg injectionNDC 00409-1703-01 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
3.5 mg injectionNDC 00409-1700-01 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
MAIA Pharmaceuticals, Inc. 2 products
1 mg injectionNDC 70511-0161-05 Sorbitol or mannitol
Show 5 ingredients

DIMETHYL SULFOXIDE, HYDROCHLORIC ACID, MANNITOL, SODIUM ACETATE, SODIUM HYDROXIDE
2.5 mg injectionNDC 70511-0162-02 Sorbitol or mannitol
Show 5 ingredients

DIMETHYL SULFOXIDE, HYDROCHLORIC ACID, MANNITOL, SODIUM ACETATE, SODIUM HYDROXIDE
Meitheal Pharmaceuticals Inc. 1 product
3.5 mg injectionNDC 71288-0118-10 Sorbitol or mannitol
Show 1 ingredient

mannitol
Ningbo Shuangcheng Pharmaceutical Co., Ltd. 1 product
3.5 mg injectionNDC 75007-0501-31 Sorbitol or mannitol
Show 1 ingredient

mannitol
NorthStar RxLLC 1 product
3.5 mg injectionNDC 72603-0270-01 Sorbitol or mannitol
Show 1 ingredient

mannitol
Novadoz Pharmaceuticals LLC 1 product
3.5 mg/3.5 mL injectionNDC 72205-0183-01 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
Pharmascience Inc. 1 product
3.5 mg injectionNDC 51817-0586-01 Still being read Not read yet
Sagent Pharmaceuticals 1 product
3.5 mg injectionNDC 25021-0262-10 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
Shilpa Medicare Limited 1 product
3.5 mg/1.4 mL injectionNDC 63759-3032-01 No inactive-ingredient list on the label No list we could read
Sintetica US LLC 1 product
3.5 mg/3.5 mL injectionNDC 83090-0008-01 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
Somerset Therapeutics LLC 1 product
3.5 mg/3.5 mL injectionNDC 70069-0836-01 Still being read Not read yet
Takeda Pharmaceuticals America, Inc. 1 product
3.5 mg injectionNDC 63020-0049-01 Still being read Not read yet
Waverley Pharma Inc 1 product
3.5 mg injectionNDC 72338-0200-01 Sorbitol or mannitol
Show 1 ingredient

mannitol
Zydus Pharmaceuticals USA Inc. 1 product
1 mg/mL injectionNDC 70710-1411-01 Sorbitol or mannitol
Show 1 ingredient

MANNITOL
Zydus Lifesciences Limited 1 product
1 mg/mL injectionNDC 70771-1708-01 Sorbitol or mannitol
Show 1 ingredient

MANNITOL

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.

Bortezomib and sorbitol or mannitol

Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. Every checked Bortezomib product (24) lists sorbitol or mannitol.

Lists sorbitol or mannitol

At the pharmacy counter

How to use this at the pharmacy counter

  1. 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.
  2. 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.
  3. 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.
  4. 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.
Ask Dr. Staiger which Bortezomib product suits you →

Common questions about Bortezomib inactive ingredients

Is Bortezomib gluten-free?
This page cannot certify any Bortezomib product gluten-free; it reports what each label declares. Of the 24 products checked, none lists a wheat, barley, rye or gluten ingredient, and none lists a starch without a stated source. If you have celiac disease, ask the manufacturer's medical information line for a written gluten statement for the lot you have.
Does Bortezomib contain lactose?
No checked Bortezomib product lists lactose on its label. People with a milk allergy or a strong intolerance often prefer a version that does not list it.
Does Bortezomib contain soy?
No checked Bortezomib product lists a soy ingredient (soybean oil or soy lecithin) on its label. Soy lecithin is the usual form and the amount is small, but people with a soy allergy often prefer a version that does not list it.
Is there a dye-free Bortezomib?
No checked Bortezomib product lists a synthetic dye (an FD&C or D&C colorant) on its label. Colorants often differ by strength within one company's line, so compare the lists above strength by strength.
Does Bortezomib contain gelatin?
No checked Bortezomib product lists gelatin on its label. Gelatin is usually bovine or porcine and the label rarely says which; for kosher, halal or vegetarian needs, ask the manufacturer.
Why do the inactive ingredients differ between manufacturers?
A generic must match the brand's active ingredient, strength and dose form. For injectable, ophthalmic and otic products the FDA generally requires the inactive ingredients to match the reference product as well, so the lists on this page differ less than they do for tablets and capsules; the differences that remain come from the exact product and container each company files.
Can my pharmacy give me a specific manufacturer's version?
Often, if you ask before the prescription is filled: many pharmacies order from wholesalers that carry several companies' versions and can request a particular one. Some pharmacies buy a generic from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check. Give them the NDC from this page; the company name alone is often enough.
How current is this list?
The products are the ones in the FDA's current NDC directory as of October 6, 2026, and each inactive-ingredient list is the manufacturer's FDA label as our label sync last read it. Formulations change, so check the label on your own bottle and ask your pharmacist if a refill looks different.

Sources: the products are the finished Bortezomib 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 Bortezomib guide