Orphenadrine inactive ingredients by manufacturer
Wondering whether your Orphenadrine 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 Orphenadrine 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 16 of the 20 current Orphenadrine products on the market today, from 17 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. 1 label has no inactive-ingredient list we could read, so that product cannot be compared.
Ask about your bottle
Is there something in your Orphenadrine? 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 Orphenadrine products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseDiffers by manufacturer
14 of 16 checked products list lactose; 2 do not. See the products
-
Wheat or gluten sourceNo checked product
No checked Orphenadrine product lists a wheat or gluten source.
-
SoyNo checked product
No checked Orphenadrine product lists soy.
-
Synthetic dyesNo checked product
No checked Orphenadrine product lists synthetic dyes.
-
GelatinNo checked product
No checked Orphenadrine product lists gelatin.
Also listed by some products: Sulfites 2 of 16
Find a version without it
Every current Orphenadrine product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| A-S Medication Solutions 1 product | ||
| 100 mg extended-release tabletNDC 50090-0169-00 | Lactose |
Show 3 ingredientsHYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| Actavis Pharma, Inc. 1 product | ||
| 30 mg/mL injectionNDC 00591-3222-47 | Still being read | Not read yet |
| Advanced Rx Pharmacy of Tennessee, LLC 2 products | ||
| 100 mg extended-release tabletNDC 80425-0117-01 | No inactive-ingredient list on the label | No list we could read |
| 100 mg extended-release tabletNDC 80425-0340-01 | Lactose |
Show 3 ingredientsHYPROMELLOSES, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| Bryant Ranch Prepack 2 products | ||
| 100 mg extended-release tabletNDC 72162-2020-01 | Lactose |
Show 3 ingredientsHYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| 100 mg extended-release tabletNDC 63629-1564-00 | Lactose |
Show 3 ingredientsHYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| Hikma Pharmaceuticals USA Inc. 1 product | ||
| 60 mg/2 mL injectionNDC 00641-6182-10 | Sulfites |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| Lake Erie Medical DBA Quality Care Products LLC 1 product | ||
| 100 mg extended-release tabletNDC 49999-0046-14 | Lactose |
Show 3 ingredientsHYPROMELLOSES, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| Lupin Pharmaceuticals, Inc. 1 product | ||
| 100 mg extended-release tabletNDC 43386-0480-24 | Lactose |
Show 3 ingredientsHYPROMELLOSES, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| Northwind Health Company, LLC 1 product | ||
| 100 mg extended-release tabletNDC 82868-0040-14 | Lactose |
Show 3 ingredientsHYPROMELLOSES, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| NuCare Pharmaceuticals, Inc. 1 product | ||
| 100 mg extended-release tabletNDC 66267-0158-20 | Lactose |
Show 3 ingredientsHYPROMELLOSES, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| PD-Rx Pharmaceuticals, Inc. 1 product | ||
| 100 mg extended-release tabletNDC 43063-0407-14 | Still being read | Not read yet |
| Preferred Pharmaceuticals, Inc. 1 product | ||
| 100 mg extended-release tabletNDC 68788-9138-01 | Lactose |
Show 3 ingredientsHYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| Proficient Rx LP 2 products | ||
| 100 mg extended-release tabletNDC 63187-0122-20 | Lactose |
Show 3 ingredientsHYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| 100 mg extended-release tabletNDC 63187-0632-30 | Lactose |
Show 3 ingredientsCALCIUM STEARATE, ETHYLCELLULOSE, UNSPECIFIED, LACTOSE MONOHYDRATE |
| RedPharm Drug 1 product | ||
| 100 mg extended-release tabletNDC 67296-1077-01 | Still being read | Not read yet |
| Remedyrepack Inc. 1 product | ||
| 100 mg extended-release tabletNDC 70518-4506-00 | Lactose |
Show 3 ingredientsHYPROMELLOSES, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
| Sagent Pharmaceuticals 1 product | ||
| 30 mg/mL injectionNDC 25021-0651-02 | Sulfites |
Show 4 ingredientssodium chloride, sodium hydroxide, sodium metabisulfite, water |
| Sandoz Inc 1 product | ||
| 100 mg extended-release tabletNDC 00185-0022-01 | Lactose |
Show 3 ingredientsCALCIUM STEARATE, ETHYLCELLULOSE, UNSPECIFIED, LACTOSE MONOHYDRATE |
| St. Mary's Medical Park Pharmacy 1 product | ||
| 100 mg extended-release tabletNDC 60760-0810-30 | Lactose |
Show 3 ingredientsHYPROMELLOSES, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE |
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.
Orphenadrine without lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 14 of 16 checked products list lactose; 2 do not.
Does not list lactose
- Hikma: 60 mg/2 mL injection
- Sagent: 30 mg/mL injection
Lists lactose
- A-S Medication Solutions: 100 mg extended-release tablet
- Advanced Rx Pharmacy of Tennessee: 100 mg extended-release tablet
- Bryant Ranch Prepack: 100 mg extended-release tablet (NDC 72162-2020-01), 100 mg extended-release tablet (NDC 63629-1564-00)
- Lake Erie Medical DBA Quality Care Products: 100 mg extended-release tablet
- Lupin: 100 mg extended-release tablet
- Northwind Health: 100 mg extended-release tablet
- NuCare: 100 mg extended-release tablet
- Preferred: 100 mg extended-release tablet
- Proficient Rx: 100 mg extended-release tablet (NDC 63187-0122-20), 100 mg extended-release tablet (NDC 63187-0632-30)
- Remedyrepack: 100 mg extended-release tablet
- Sandoz: 100 mg extended-release tablet
- St. Mary's Medical Park Pharmacy: 100 mg extended-release tablet
Orphenadrine without sulfites
Sulfites: metabisulfite or bisulfite preservatives; a concern with sulfite sensitivity or asthma. 2 of 16 checked products list sulfites; 14 do not.
Does not list sulfites
- A-S Medication Solutions: 100 mg extended-release tablet
- Advanced Rx Pharmacy of Tennessee: 100 mg extended-release tablet
- Bryant Ranch Prepack: 100 mg extended-release tablet (NDC 72162-2020-01), 100 mg extended-release tablet (NDC 63629-1564-00)
- Lake Erie Medical DBA Quality Care Products: 100 mg extended-release tablet
- Lupin: 100 mg extended-release tablet
- Northwind Health: 100 mg extended-release tablet
- NuCare: 100 mg extended-release tablet
- Preferred: 100 mg extended-release tablet
- Proficient Rx: 100 mg extended-release tablet (NDC 63187-0122-20), 100 mg extended-release tablet (NDC 63187-0632-30)
- Remedyrepack: 100 mg extended-release tablet
- Sandoz: 100 mg extended-release tablet
- St. Mary's Medical Park Pharmacy: 100 mg extended-release tablet
Lists sulfites
- Hikma: 60 mg/2 mL injection
- Sagent: 30 mg/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 Orphenadrine inactive ingredients
Is Orphenadrine gluten-free?
Does Orphenadrine contain lactose?
Does Orphenadrine contain soy?
Is there a dye-free Orphenadrine?
Does Orphenadrine 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 Orphenadrine 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 Orphenadrine guide