Inactive ingredients by manufacturer

Thiotepa Injection inactive ingredients by manufacturer

Wondering whether your Thiotepa 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 Thiotepa 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 9 of the 19 current Thiotepa Injection products on the market today, from 9 companies listing it with the FDA, and lined them up side by side. 8 labels have no inactive-ingredient list we could read, so those products cannot be compared. 2 could not be linked to a current label.

Ask about your bottle

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

  1. LactoseNo checked product

    No checked Thiotepa Injection product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Thiotepa Injection product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Thiotepa Injection product lists soy.

  4. Synthetic dyesNo checked product

    No checked Thiotepa Injection product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Thiotepa Injection product lists gelatin.

Find a version without it

Every current Thiotepa Injection product and what its label lists

No checked product lists any of the concerns we look for.

ProductListsInactive ingredients on the label
Amneal Pharmaceuticals LLC 4 products
15 mg injectionNDC 70121-1630-01 No inactive-ingredient list on the label No list we could read
100 mg injectionNDC 70121-1631-01 No inactive-ingredient list on the label No list we could read
200 mg injectionNDC 70121-2749-01 None of these listed
Show 1 ingredient

SODIUM CHLORIDE
400 mg injectionNDC 70121-1687-01 None of these listed
Show 1 ingredient

SODIUM CHLORIDE
Dr.Reddy's Laboratories Inc., 2 products
15 mg injectionNDC 43598-0650-11 None of these listed
Show 1 ingredient

Water
100 mg injectionNDC 43598-0171-11 No inactive-ingredient list on the label No list we could read
Fresenius Kabi USA, LLC 1 product
100 mg injectionNDC 65219-0029-20 None of these listed
Show 1 ingredient

WATER
Gland Pharma Limited 2 products
15 mg injectionNDC 68083-0446-01 None of these listed
Show 1 ingredient

WATER
100 mg injectionNDC 68083-0503-01 None of these listed
Show 1 ingredient

WATER
Hikma Pharmaceuticals USA Inc. 3 products
15 mg/1.5 mL injectionNDC 00143-9309-01 None of these listed
Show 1 ingredient

WATER
15 mg/1.5 mL injectionNDC 00143-9565-01 None of these listed
Show 1 ingredient

WATER
100 mg injectionNDC 00143-9292-01 None of these listed
Show 1 ingredient

WATER
Meitheal Pharmaceuticals Inc 2 products
15 mg injectionNDC 71288-0156-05 No inactive-ingredient list on the label No list we could read
100 mg injectionNDC 71288-0157-10 No inactive-ingredient list on the label No list we could read
Novadoz Pharmaceuticals LLC 2 products
15 mg injectionNDC 72205-0045-01 No inactive-ingredient list on the label No list we could read
100 mg injectionNDC 72205-0046-01 No inactive-ingredient list on the label No list we could read
Sagent Pharmaceuticals 1 product
15 mg/1.5 mL injectionNDC 25021-0246-02 No inactive-ingredient list on the label No list we could read
Shorla Oncology Inc. 2 products
10 mg/mL injectionNDC 81927-0106-01 No current label Not available
10 mg/mL injectionNDC 81927-0105-01 No current label Not available

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.

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 Thiotepa Injection product suits you →

Common questions about Thiotepa Injection inactive ingredients

Is Thiotepa Injection gluten-free?
This page cannot certify any Thiotepa Injection product gluten-free; it reports what each label declares. Of the 9 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 Thiotepa Injection contain lactose?
No checked Thiotepa Injection 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 Thiotepa Injection contain soy?
No checked Thiotepa Injection 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 Thiotepa Injection?
No checked Thiotepa Injection 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 Thiotepa Injection contain gelatin?
No checked Thiotepa Injection 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 Thiotepa 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 Thiotepa Injection guide