Inactive ingredients by manufacturer

Rufinamide inactive ingredients by manufacturer

Wondering whether your Rufinamide 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 Rufinamide 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 21 of the 24 current Rufinamide products on the market today, from 12 companies listing it with the FDA, and lined them up side by side. 3 are still being read and will appear on a later visit.

Ask about your bottle

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

  1. LactoseDiffers by manufacturer
  2. Wheat or gluten sourceNo checked product

    No checked Rufinamide product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Rufinamide product lists soy.

  4. Synthetic dyesNo checked product

    No checked Rufinamide product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Rufinamide product lists gelatin.

Also listed by some products: Corn 11 of 21 Titanium dioxide 12 of 21 Propylene glycol 7 of 21 PEG or polysorbate 19 of 21 Sorbitol or mannitol 9 of 21

Find a version without it

Every current Rufinamide product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
American Health Packaging 1 product
40 mg/mL oral suspensionNDC 60687-0824-08 Polyethylene glycol or polysorbate Sorbitol or mannitol
Show 13 ingredients

1-PROPOXY-2-PROPANOL, ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED, DIMETHICONE 350, HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%), METHYLPARABEN, MICROCRYSTALLINE CELLULOSE, POLOXAMER 188, POTASSIUM SORBATE, PROPYLPARABEN, SODIUM HYDROXIDE, SORBITOL, WATER

Ascend Laboratories, LLC 1 product
40 mg/mL oral suspensionNDC 67877-0673-62 Lactose Propylene glycol Sorbitol or mannitol
Show 15 ingredients

ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED, DIMETHICONE, HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%), HYPROMELLOSE 2910 (5 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, METHYLPARABEN, MICROCRYSTALLINE CELLULOSE, ORANGE, POTASSIUM SORBATE, PROPYLENE GLYCOL, PROPYLPARABEN, SILICON DIOXIDE, SORBITOL

Aurobindo Pharma Limited 3 products
40 mg/mL oral suspensionNDC 59651-0563-60 Propylene glycol Polyethylene glycol or polysorbate Sorbitol or mannitol
Show 13 ingredients

.ALPHA.-TOCOPHEROL, DL-, ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED, DIMETHICONE, HYDROXYETHYL CELLULOSE, UNSPECIFIED, METHYLPARABEN, MICROCRYSTALLINE CELLULOSE, NONCRYSTALLIZING SORBITOL SOLUTION, POLOXAMER 188, POTASSIUM SORBATE, PROPYLENE GLYCOL, PROPYLPARABEN, WATER

200 mg tabletNDC 59651-0616-08 Lactose Corn-derived Titanium dioxide Polyethylene glycol or polysorbate
Show 13 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2910 (5 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 4000, SILICON DIOXIDE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

400 mg tabletNDC 59651-0617-08 Lactose Corn-derived Titanium dioxide Polyethylene glycol or polysorbate
Show 13 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2910 (5 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 4000, SILICON DIOXIDE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

Bionpharma Inc. 1 product
40 mg/mL oral suspensionNDC 69452-0223-84 Propylene glycol Polyethylene glycol or polysorbate Sorbitol or mannitol
Show 15 ingredients

ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM, CELLULOSE, MICROCRYSTALLINE, DIMETHICONE, HYDROCHLORIC ACID, HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%), METHYLPARABEN, ORANGE, POLOXAMER 188, POTASSIUM SORBATE, PROPYLENE GLYCOL, PROPYLPARABEN, SODIUM HYDROXIDE, SORBITOL, WATER

Camber Pharmaceuticals, Inc. 3 products
40 mg/mL oral suspensionNDC 31722-0688-46 Propylene glycol Polyethylene glycol or polysorbate Sorbitol or mannitol
Show 13 ingredients

ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED, DIMETHICONE, HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%), METHYLPARABEN, MICROCRYSTALLINE CELLULOSE, NONCRYSTALLIZING SORBITOL SOLUTION, ORANGE, POLOXAMER 188, POTASSIUM SORBATE, PROPYLENE GLYCOL, PROPYLPARABEN, WATER

200 mg tabletNDC 31722-0598-12 Still being read Not read yet
400 mg tabletNDC 31722-0599-12 Lactose Titanium dioxide Polyethylene glycol or polysorbate
Show 11 ingredients

CROSPOVIDONE, FERRIC OXIDE RED, HYPROMELLOSE 2910 (3 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 400, POLYSORBATE 80, SILICON DIOXIDE, SODIUM LAURYL SULFATE, TITANIUM DIOXIDE

Eisai Inc. 3 products
40 mg/mL oral suspensionNDC 62856-0584-46 Propylene glycol Polyethylene glycol or polysorbate Sorbitol or mannitol
Show 14 ingredients

ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM, CELLULOSE, MICROCRYSTALLINE, DIMETHICONE, HYDROXYETHYL CELLULOSE (2000 CPS AT 1%), METHYLPARABEN, ORANGE, POLOXAMER 188, POTASSIUM SORBATE, PROPYLENE GLYCOL, PROPYLPARABEN, SILICON DIOXIDE, SORBITOL, WATER

200 mg tabletNDC 62856-0582-04 Lactose Corn-derived Titanium dioxide Polyethylene glycol or polysorbate
Show 13 ingredients

CELLULOSE, MICROCRYSTALLINE, CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2208 (3 MPA.S), HYPROMELLOSE 2910 (3 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 8000, SILICON DIOXIDE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

400 mg tabletNDC 62856-0583-14 Lactose Corn-derived Titanium dioxide Polyethylene glycol or polysorbate
Show 13 ingredients

CELLULOSE, MICROCRYSTALLINE, CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2208 (3 MPA.S), HYPROMELLOSE 2910 (3 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 8000, SILICON DIOXIDE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

Glenmark Pharmaceuticals Inc., USA 2 products
200 mg tabletNDC 68462-0713-05 Lactose Corn-derived Titanium dioxide Polyethylene glycol or polysorbate
Show 12 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2910 (5 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL, UNSPECIFIED, SILICON DIOXIDE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

400 mg tabletNDC 68462-0714-05 Lactose Corn-derived Titanium dioxide Polyethylene glycol or polysorbate
Show 12 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2910 (5 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL, UNSPECIFIED, SILICON DIOXIDE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

Hikma Pharmaceuticals USA Inc. 3 products
40 mg/mL oral suspensionNDC 00054-0528-63 Polyethylene glycol or polysorbate Sorbitol or mannitol
Show 13 ingredients

1-PROPOXY-2-PROPANOL, ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM, DIMETHICONE 350, HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%), METHYLPARABEN, MICROCRYSTALLINE CELLULOSE, POLOXAMER 188, POTASSIUM SORBATE, PROPYLPARABEN, SODIUM HYDROXIDE, SORBITOL, WATER

200 mg tabletNDC 00054-0425-23 Still being read Not read yet
400 mg tabletNDC 00054-0426-23 Lactose Corn-derived Titanium dioxide
Show 11 ingredients

1-PROPOXY-2-PROPANOL, CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2208 (100 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

Lupin Pharmaceuticals, Inc. 3 products
40 mg/mL oral suspensionNDC 68180-0797-01 Still being read Not read yet
200 mg tabletNDC 68180-0803-06 Lactose Corn-derived Titanium dioxide Polyethylene glycol or polysorbate
Show 12 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2910 (3 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 400, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

400 mg tabletNDC 68180-0804-16 Lactose Corn-derived Titanium dioxide Polyethylene glycol or polysorbate
Show 12 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2910 (3 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 400, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

Micro Labs Limited 2 products
200 mg tabletNDC 42571-0391-12 Lactose Corn-derived Titanium dioxide Polyethylene glycol or polysorbate
Show 14 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2208 (100 MPA.S), HYPROMELLOSE 2208 (3 MPA.S), HYPROMELLOSE 2910 (3 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 8000, SILICON DIOXIDE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

400 mg tabletNDC 42571-0392-12 Lactose Corn-derived Titanium dioxide Polyethylene glycol or polysorbate
Show 14 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, HYPROMELLOSE 2208 (100 MPA.S), HYPROMELLOSE 2208 (3 MPA.S), HYPROMELLOSE 2910 (3 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 8000, SILICON DIOXIDE, SODIUM LAURYL SULFATE, STARCH, CORN, TALC, TITANIUM DIOXIDE

NorthStar RxLLC 1 product
40 mg/mL oral suspensionNDC 72603-0261-01 Propylene glycol Polyethylene glycol or polysorbate Sorbitol or mannitol
Show 13 ingredients

ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED, DIMETHICONE, HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%), METHYLPARABEN, MICROCRYSTALLINE CELLULOSE, NONCRYSTALLIZING SORBITOL SOLUTION, ORANGE, POLOXAMER 188, POTASSIUM SORBATE, PROPYLENE GLYCOL, PROPYLPARABEN, WATER

Novadoz Pharmaceuticals LLC 1 product
40 mg/mL oral suspensionNDC 72205-0038-77 Propylene glycol Polyethylene glycol or polysorbate Sorbitol or mannitol
Show 14 ingredients

ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM, CELLULOSE, MICROCRYSTALLINE, DIMETHICONE, UNSPECIFIED, METHYLPARABEN, ORANGE, POLOXAMER 188, POTASSIUM SORBATE, PROPYLENE GLYCOL, PROPYLPARABEN, SILICON DIOXIDE, SORBITOL, TRIACETIN, XANTHAN GUM

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.

Rufinamide without lactose

Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 13 of 21 checked products list lactose; 8 do not.

Rufinamide without corn-derived ingredients

Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. 11 of 21 checked products list corn-derived ingredients; 10 do not.

Does not list corn-derived ingredients

Lists corn-derived ingredients

Rufinamide without titanium dioxide

Titanium dioxide: A white colorant some people choose to avoid. 12 of 21 checked products list titanium dioxide; 9 do not.

Rufinamide without propylene glycol

Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 7 of 21 checked products list propylene glycol; 14 do not.

Rufinamide without polyethylene glycol or polysorbate

Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. 19 of 21 checked products list polyethylene glycol or polysorbate; 2 do not.

Does not list polyethylene glycol or polysorbate

Rufinamide without sorbitol or mannitol

Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 9 of 21 checked products list sorbitol or mannitol; 12 do not.

Does not list 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 Rufinamide product suits you →

Common questions about Rufinamide inactive ingredients

Is Rufinamide gluten-free?
This page cannot certify any Rufinamide product gluten-free; it reports what each label declares. Of the 21 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 Rufinamide contain lactose?
13 of 21 checked Rufinamide products list lactose; 8 do not: American Health Packaging (40 mg/mL oral suspension), Aurobindo (40 mg/mL oral suspension), Bionpharma (40 mg/mL oral suspension) and Camber (40 mg/mL oral suspension) and 4 other companies. The lactose in a tablet or capsule is a small amount, but people with a milk allergy or a strong intolerance often prefer a version that does not list it.
Does Rufinamide contain soy?
No checked Rufinamide 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 Rufinamide?
No checked Rufinamide 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 Rufinamide contain gelatin?
No checked Rufinamide 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, dose form and how it is absorbed; its fillers, binders, coatings and colorants are the manufacturer's own choice. That is why one Rufinamide product can list lactose and a dye while another from a different company lists neither.
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 Rufinamide 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 Rufinamide guide