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?
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LactoseNo checked product
No checked Pemetrexed Disodium product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Pemetrexed Disodium product lists a wheat or gluten source.
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SoyNo checked product
No checked Pemetrexed Disodium product lists soy.
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Synthetic dyesNo checked product
No checked Pemetrexed Disodium product lists synthetic dyes.
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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
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Amneal Pharmaceuticals LLC 3 products | ||
| 100 mg/10 mL injectionNDC 70121-2453-01 | Sorbitol or mannitol |
Show 5 ingredientsCYSTEINE HYDROCHLORIDE, HYDROCHLORIC ACID, MANNITOL, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| 500 mg/50 mL injectionNDC 70121-2461-01 | Sorbitol or mannitol |
Show 5 ingredientsCYSTEINE 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 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| 100 mg/4 mL injectionNDC 68001-0538-41 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| 500 mg/20 mL injectionNDC 68001-0539-41 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| 500 mg/20 mL injectionNDC 68001-0544-41 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC 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 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| Camber Pharmaceuticals, Inc. 2 products | ||
| 100 mg/4 mL injectionNDC 31722-0336-31 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| 500 mg/20 mL injectionNDC 31722-0337-31 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| Dr. Reddys Laboratories Inc 3 products | ||
| 1 g/40 mL injectionNDC 43598-0370-74 | Sorbitol or mannitol |
Show 3 ingredientsHydrochloric acid, Mannitol, Sodium Hydroxide |
| 100 mg/4 mL injectionNDC 43598-0386-62 | Sorbitol or mannitol |
Show 3 ingredientsHydrochloric acid, Mannitol, Sodium Hydroxide |
| 500 mg/20 mL injectionNDC 43598-0387-11 | Sorbitol or mannitol |
Show 3 ingredientsHydrochloric acid, Mannitol, Sodium Hydroxide |
| Eli Lilly and Company 2 products | ||
| 100 mg/4 mL injectionNDC 00002-7640-01 | Sorbitol or mannitol |
Show 3 ingredientsHydrochloric acid, Mannitol, Sodium hydroxide |
| 500 mg/20 mL injectionNDC 00002-7623-01 | Sorbitol or mannitol |
Show 3 ingredientsHydrochloric acid, Mannitol, Sodium hydroxide |
| Fresenius Kabi USA, LLC 4 products | ||
| 1 g/40 mL injectionNDC 63323-0622-00 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| 100 mg/4 mL injectionNDC 63323-0134-10 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| 500 mg/20 mL injectionNDC 63323-0450-50 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| 750 mg/30 mL injectionNDC 63323-0621-00 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| Meitheal Pharmaceuticals Inc. 6 products | ||
| 1 g/40 mL injectionNDC 71288-0148-51 | Sorbitol or mannitol |
Show 3 ingredientshydrochloric acid, mannitol, sodium hydroxide |
| 100 mg/4.2 mL injectionNDC 71288-0145-10 | Sorbitol or mannitol |
Show 3 ingredientshydrochloric acid, mannitol, sodium hydroxide |
| 100 mg/10 mL injectionNDC 71288-0166-10 | Sorbitol or mannitol |
Show 3 ingredientshydrochloric acid, mannitol, sodium hydroxide |
| 500 mg/20 mL injectionNDC 71288-0146-50 | Sorbitol or mannitol |
Show 3 ingredientshydrochloric acid, mannitol, sodium hydroxide |
| 500 mg/50 mL injectionNDC 71288-0167-50 | Sorbitol or mannitol |
Show 3 ingredientshydrochloric 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 ingredientshydrochloric acid, mannitol, sodium hydroxide |
| 500 mg/50 mL injectionNDC 72603-0425-01 | Sorbitol or mannitol |
Show 3 ingredientshydrochloric acid, mannitol, sodium hydroxide |
| Qilu Pharmaceutical Co., Ltd. 2 products | ||
| 100 mg/4 mL injectionNDC 67184-0503-01 | Sorbitol or mannitol |
Show 3 ingredientsHydrochloric 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 ingredientsHydrochloric Acid, Mannitol, Sodium Hydroxide |
| 500 mg/20 mL injectionNDC 25021-0261-50 | Sorbitol or mannitol |
Show 3 ingredientsHydrochloric Acid, Mannitol, Sodium Hydroxide |
| Sandoz Inc. 2 products | ||
| 100 mg/4 mL injectionNDC 00781-3518-76 | Propylene glycol |
Show 5 ingredientsHYDROCHLORIC ACID, PROPYLENE GLYCOL, SODIUM HYDROXIDE, SODIUM THIOSULFATE, WATER |
| 500 mg/20 mL injectionNDC 00781-3519-90 | Propylene glycol |
Show 5 ingredientsHYDROCHLORIC 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 ingredientsCYSTEINE HYDROCHLORIDE, HYDROCHLORIC ACID, MANNITOL, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| 500 mg/50 mL injectionNDC 63759-3049-01 | Sorbitol or mannitol |
Show 5 ingredientsCYSTEINE HYDROCHLORIDE, HYDROCHLORIC ACID, MANNITOL, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| 1000 mg/100 mL injectionNDC 63759-3050-01 | Sorbitol or mannitol |
Show 5 ingredientsCYSTEINE 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 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| Waverley Pharma Inc 2 products | ||
| 100 mg/4 mL injectionNDC 72338-0100-01 | Sorbitol or mannitol |
Show 3 ingredientsHydrochloric acid, Mannitol, Sodium hydroxide |
| 500 mg/20 mL injectionNDC 72338-0101-01 | Sorbitol or mannitol |
Show 3 ingredientsHydrochloric acid, Mannitol, Sodium hydroxide |
| Zydus Pharmaceuticals USA Inc. 3 products | ||
| 100 mg/4 mL injectionNDC 70710-1654-01 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| 500 mg/20 mL injectionNDC 70710-1655-01 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC 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 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| 500 mg/20 mL injectionNDC 70771-1692-01 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE |
| 1000 mg/40 mL injectionNDC 70771-1693-01 | Sorbitol or mannitol |
Show 3 ingredientsHYDROCHLORIC 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.
Does not list propylene glycol
- Amneal: 100 mg/10 mL injection, 500 mg/50 mL injection
- BluePoint: 100 mg/4 mL injection (NDC 68001-0543-41), 100 mg/4 mL injection (NDC 68001-0538-41), 500 mg/20 mL injection (NDC 68001-0539-41), 500 mg/20 mL injection (NDC 68001-0544-41), 1000 mg/40 mL injection
- Camber: 100 mg/4 mL injection, 500 mg/20 mL injection
- Dr. Reddys: 1 g/40 mL injection, 100 mg/4 mL injection, 500 mg/20 mL injection
- Eli Lilly and: 100 mg/4 mL injection, 500 mg/20 mL injection
- Fresenius Kabi: 1 g/40 mL injection, 100 mg/4 mL injection, 500 mg/20 mL injection, 750 mg/30 mL injection
- Meitheal: 1 g/40 mL injection, 100 mg/4.2 mL injection, 100 mg/10 mL injection, 500 mg/20 mL injection, 500 mg/50 mL injection
- NorthStar RxLLC: 100 mg/10 mL injection, 500 mg/50 mL injection
- Qilu: 100 mg/4 mL injection
- Sagent: 100 mg/4.2 mL injection, 500 mg/20 mL injection
- Shilpa Medicare: 100 mg/10 mL injection, 500 mg/50 mL injection, 1000 mg/100 mL injection
- Somerset Therapeutics: 500 mg/20 mL injection
- Waverley: 100 mg/4 mL injection, 500 mg/20 mL injection
- Zydus: 100 mg/4 mL injection, 500 mg/20 mL injection
- Zydus Lifesciences: 100 mg/4 mL injection, 500 mg/20 mL injection, 1000 mg/40 mL injection
Lists propylene glycol
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.
Does not list sorbitol or mannitol
Lists sorbitol or mannitol
- Amneal: 100 mg/10 mL injection, 500 mg/50 mL injection
- BluePoint: 100 mg/4 mL injection (NDC 68001-0543-41), 100 mg/4 mL injection (NDC 68001-0538-41), 500 mg/20 mL injection (NDC 68001-0539-41), 500 mg/20 mL injection (NDC 68001-0544-41), 1000 mg/40 mL injection
- Camber: 100 mg/4 mL injection, 500 mg/20 mL injection
- Dr. Reddys: 1 g/40 mL injection, 100 mg/4 mL injection, 500 mg/20 mL injection
- Eli Lilly and: 100 mg/4 mL injection, 500 mg/20 mL injection
- Fresenius Kabi: 1 g/40 mL injection, 100 mg/4 mL injection, 500 mg/20 mL injection, 750 mg/30 mL injection
- Meitheal: 1 g/40 mL injection, 100 mg/4.2 mL injection, 100 mg/10 mL injection, 500 mg/20 mL injection, 500 mg/50 mL injection
- NorthStar RxLLC: 100 mg/10 mL injection, 500 mg/50 mL injection
- Qilu: 100 mg/4 mL injection
- Sagent: 100 mg/4.2 mL injection, 500 mg/20 mL injection
- Shilpa Medicare: 100 mg/10 mL injection, 500 mg/50 mL injection, 1000 mg/100 mL injection
- Somerset Therapeutics: 500 mg/20 mL injection
- Waverley: 100 mg/4 mL injection, 500 mg/20 mL injection
- Zydus: 100 mg/4 mL injection, 500 mg/20 mL injection
- Zydus Lifesciences: 100 mg/4 mL injection, 500 mg/20 mL injection, 1000 mg/40 mL injection
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 Pemetrexed Disodium inactive ingredients
Is Pemetrexed Disodium gluten-free?
Does Pemetrexed Disodium contain lactose?
Does Pemetrexed Disodium contain soy?
Is there a dye-free Pemetrexed Disodium?
Does Pemetrexed Disodium 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 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