Inactive ingredients by manufacturer

Epoprostenol inactive ingredients by manufacturer

Wondering whether your Epoprostenol 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 Epoprostenol 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 4 of the 8 current Epoprostenol products on the market today, from 4 companies listing it with the FDA, and lined them up side by side. 4 are still being read and will appear on a later visit.

Ask about your bottle

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

  1. LactoseNo checked product

    No checked Epoprostenol product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Epoprostenol product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Epoprostenol product lists soy.

  4. Synthetic dyesNo checked product

    No checked Epoprostenol product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Epoprostenol product lists gelatin.

Also listed by some products: Sugar 4 of 4

Find a version without it

Every current Epoprostenol product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
Actelion Pharmaceuticals US, Inc. 2 products
0.5 mg/10 mL injectionNDC 66215-0403-01 Still being read Not read yet
1.5 mg/10 mL injectionNDC 66215-0402-01 Sugar (sucrose, dextrose)
Show 3 ingredients

arginine, sodium hydroxide, sucrose
Gland Pharma Limited 2 products
0.5 mg/10 mL injectionNDC 68083-0707-01 Still being read Not read yet
1.5 mg/10 mL injectionNDC 68083-0642-01 Still being read Not read yet
Mylan Institutional LLC 2 products
0.5 mg/10 mL injectionNDC 67457-0587-10 Sugar (sucrose, dextrose)
Show 3 ingredients

ARGININE, SODIUM HYDROXIDE, SUCROSE
1.5 mg/10 mL injectionNDC 67457-0588-10 Still being read Not read yet
Sun Pharmaceutical Industries, Inc. 2 products
0.5 mg/10 mL injectionNDC 62756-0059-40 Sugar (sucrose, dextrose)
Show 3 ingredients

GLYCINE, SODIUM HYDROXIDE, SUCROSE
1.5 mg/10 mL injectionNDC 62756-0060-40 Sugar (sucrose, dextrose)
Show 3 ingredients

GLYCINE, SODIUM HYDROXIDE, SUCROSE

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.

Epoprostenol and sugar (sucrose or dextrose)

Sugar (sucrose, dextrose): A consideration in diabetes, mostly in liquids and chewables. Every checked Epoprostenol product (4) lists sugar (sucrose or dextrose).

Lists sugar (sucrose or dextrose)

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 Epoprostenol product suits you →

Common questions about Epoprostenol inactive ingredients

Is Epoprostenol gluten-free?
This page cannot certify any Epoprostenol product gluten-free; it reports what each label declares. Of the 4 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 Epoprostenol contain lactose?
No checked Epoprostenol 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 Epoprostenol contain soy?
No checked Epoprostenol 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 Epoprostenol?
No checked Epoprostenol 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 Epoprostenol contain gelatin?
No checked Epoprostenol 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 Epoprostenol 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 Epoprostenol guide