Inactive ingredients by manufacturer

Pemetrexed Disodium inactive ingredients by manufacturer

Wondering whether your Pemetrexed Disodium 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 Pemetrexed Disodium 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 41 of the 47 current Pemetrexed Disodium products on the market today, from 16 companies listing it with the FDA, and lined them up side by side. The FDA directory lists 48 current products in all; this page covers the 47 we hold labels for. 6 are still being read and will appear on a later visit.

Ask about your bottle

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

  1. LactoseNo checked product

    No checked Pemetrexed Disodium product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Pemetrexed Disodium product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Pemetrexed Disodium product lists soy.

  4. Synthetic dyesNo checked product

    No checked Pemetrexed Disodium product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Pemetrexed Disodium product lists gelatin.

Also listed by some products: Propylene glycol 2 of 41 Sorbitol or mannitol 39 of 41

Find a version without it

Current Pemetrexed Disodium products in our label sample and what each label lists

Hide products that list:

ProductListsInactive ingredients on the label
Amneal Pharmaceuticals LLC 3 products
100 mg/10 mL injectionNDC 70121-2453-01 Sorbitol or mannitol
Show 5 ingredients

CYSTEINE HYDROCHLORIDE, HYDROCHLORIC ACID, MANNITOL, SODIUM CHLORIDE, SODIUM HYDROXIDE

500 mg/50 mL injectionNDC 70121-2461-01 Sorbitol or mannitol
Show 5 ingredients

CYSTEINE HYDROCHLORIDE, HYDROCHLORIC ACID, MANNITOL, SODIUM CHLORIDE, SODIUM HYDROXIDE

1000 mg/100 mL injectionNDC 70121-2462-01 Still being read Not read yet
BluePoint Laboratories 6 products
100 mg/4 mL injectionNDC 68001-0543-41 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

100 mg/4 mL injectionNDC 68001-0538-41 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

500 mg/20 mL injectionNDC 68001-0539-41 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

500 mg/20 mL injectionNDC 68001-0544-41 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

750 mg/30 mL injectionNDC 68001-0545-41 Still being read Not read yet
1000 mg/40 mL injectionNDC 68001-0546-41 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

Camber Pharmaceuticals, Inc. 2 products
100 mg/4 mL injectionNDC 31722-0336-31 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

500 mg/20 mL injectionNDC 31722-0337-31 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

Dr. Reddys Laboratories Inc 3 products
1 g/40 mL injectionNDC 43598-0370-74 Sorbitol or mannitol
Show 3 ingredients

Hydrochloric acid, Mannitol, Sodium Hydroxide

100 mg/4 mL injectionNDC 43598-0386-62 Sorbitol or mannitol
Show 3 ingredients

Hydrochloric acid, Mannitol, Sodium Hydroxide

500 mg/20 mL injectionNDC 43598-0387-11 Sorbitol or mannitol
Show 3 ingredients

Hydrochloric acid, Mannitol, Sodium Hydroxide

Eli Lilly and Company 2 products
100 mg/4 mL injectionNDC 00002-7640-01 Sorbitol or mannitol
Show 3 ingredients

Hydrochloric acid, Mannitol, Sodium hydroxide

500 mg/20 mL injectionNDC 00002-7623-01 Sorbitol or mannitol
Show 3 ingredients

Hydrochloric acid, Mannitol, Sodium hydroxide

Fresenius Kabi USA, LLC 4 products
1 g/40 mL injectionNDC 63323-0622-00 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

100 mg/4 mL injectionNDC 63323-0134-10 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

500 mg/20 mL injectionNDC 63323-0450-50 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

750 mg/30 mL injectionNDC 63323-0621-00 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

Meitheal Pharmaceuticals Inc. 6 products
1 g/40 mL injectionNDC 71288-0148-51 Sorbitol or mannitol
Show 3 ingredients

hydrochloric acid, mannitol, sodium hydroxide

100 mg/4.2 mL injectionNDC 71288-0145-10 Sorbitol or mannitol
Show 3 ingredients

hydrochloric acid, mannitol, sodium hydroxide

100 mg/10 mL injectionNDC 71288-0166-10 Sorbitol or mannitol
Show 3 ingredients

hydrochloric acid, mannitol, sodium hydroxide

500 mg/20 mL injectionNDC 71288-0146-50 Sorbitol or mannitol
Show 3 ingredients

hydrochloric acid, mannitol, sodium hydroxide

500 mg/50 mL injectionNDC 71288-0167-50 Sorbitol or mannitol
Show 3 ingredients

hydrochloric acid, mannitol, sodium hydroxide

750 mg/30 mL injectionNDC 71288-0147-50 Still being read Not read yet
NorthStar RxLLC 2 products
100 mg/10 mL injectionNDC 72603-0325-01 Sorbitol or mannitol
Show 3 ingredients

hydrochloric acid, mannitol, sodium hydroxide

500 mg/50 mL injectionNDC 72603-0425-01 Sorbitol or mannitol
Show 3 ingredients

hydrochloric acid, mannitol, sodium hydroxide

Qilu Pharmaceutical Co., Ltd. 2 products
100 mg/4 mL injectionNDC 67184-0503-01 Sorbitol or mannitol
Show 3 ingredients

Hydrochloric acid, Mannitol, Sodium hydroxide

500 mg/20 mL injectionNDC 67184-0504-01 Still being read Not read yet
Sagent Pharmaceuticals 2 products
100 mg/4.2 mL injectionNDC 25021-0260-10 Sorbitol or mannitol
Show 3 ingredients

Hydrochloric Acid, Mannitol, Sodium Hydroxide

500 mg/20 mL injectionNDC 25021-0261-50 Sorbitol or mannitol
Show 3 ingredients

Hydrochloric Acid, Mannitol, Sodium Hydroxide

Sandoz Inc. 2 products
100 mg/4 mL injectionNDC 00781-3518-76 Propylene glycol
Show 5 ingredients

HYDROCHLORIC ACID, PROPYLENE GLYCOL, SODIUM HYDROXIDE, SODIUM THIOSULFATE, WATER

500 mg/20 mL injectionNDC 00781-3519-90 Propylene glycol
Show 5 ingredients

HYDROCHLORIC ACID, PROPYLENE GLYCOL, SODIUM HYDROXIDE, SODIUM THIOSULFATE, WATER

Shilpa Medicare Limited 3 products
100 mg/10 mL injectionNDC 63759-3048-01 Sorbitol or mannitol
Show 5 ingredients

CYSTEINE HYDROCHLORIDE, HYDROCHLORIC ACID, MANNITOL, SODIUM CHLORIDE, SODIUM HYDROXIDE

500 mg/50 mL injectionNDC 63759-3049-01 Sorbitol or mannitol
Show 5 ingredients

CYSTEINE HYDROCHLORIDE, HYDROCHLORIC ACID, MANNITOL, SODIUM CHLORIDE, SODIUM HYDROXIDE

1000 mg/100 mL injectionNDC 63759-3050-01 Sorbitol or mannitol
Show 5 ingredients

CYSTEINE HYDROCHLORIDE, HYDROCHLORIC ACID, MANNITOL, SODIUM CHLORIDE, SODIUM HYDROXIDE

Somerset Therapeutics LLC 2 products
100 mg/4 mL injectionNDC 70069-0834-01 Still being read Not read yet
500 mg/20 mL injectionNDC 70069-0835-01 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

Waverley Pharma Inc 2 products
100 mg/4 mL injectionNDC 72338-0100-01 Sorbitol or mannitol
Show 3 ingredients

Hydrochloric acid, Mannitol, Sodium hydroxide

500 mg/20 mL injectionNDC 72338-0101-01 Sorbitol or mannitol
Show 3 ingredients

Hydrochloric acid, Mannitol, Sodium hydroxide

Zydus Pharmaceuticals USA Inc. 3 products
100 mg/4 mL injectionNDC 70710-1654-01 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

500 mg/20 mL injectionNDC 70710-1655-01 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

1000 mg/40 mL injectionNDC 70710-1674-01 Still being read Not read yet
Zydus Lifesciences Limited 3 products
100 mg/4 mL injectionNDC 70771-1691-01 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

500 mg/20 mL injectionNDC 70771-1692-01 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

1000 mg/40 mL injectionNDC 70771-1693-01 Sorbitol or mannitol
Show 3 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE

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.

Pemetrexed Disodium without propylene glycol

Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 2 of 41 checked products list propylene glycol; 39 do not.

Pemetrexed Disodium without sorbitol or mannitol

Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 39 of 41 checked products list sorbitol or mannitol; 2 do not.

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 Pemetrexed Disodium product suits you →

Common questions about Pemetrexed Disodium inactive ingredients

Is Pemetrexed Disodium gluten-free?
This page cannot certify any Pemetrexed Disodium product gluten-free; it reports what each label declares. Of the 41 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 Pemetrexed Disodium contain lactose?
No checked Pemetrexed Disodium 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 Pemetrexed Disodium contain soy?
No checked Pemetrexed Disodium 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 Pemetrexed Disodium?
No checked Pemetrexed Disodium 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 Pemetrexed Disodium contain gelatin?
No checked Pemetrexed Disodium 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 5, 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 Pemetrexed Disodium 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 Pemetrexed Disodium guide