Sodium Oxybate inactive ingredients by manufacturer
Wondering whether your Sodium Oxybate 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 Sodium Oxybate 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 3 of the 10 current Sodium Oxybate products on the market today, from 6 companies listing it with the FDA, and lined them up side by side. 6 labels have no inactive-ingredient list we could read, so those products cannot be compared. 1 could not be linked to a current label.
Ask about your bottle
Is there something in your Sodium Oxybate? 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 Sodium Oxybate products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Sodium Oxybate product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Sodium Oxybate product lists a wheat or gluten source.
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SoyNo checked product
No checked Sodium Oxybate product lists soy.
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Synthetic dyesNo checked product
No checked Sodium Oxybate product lists synthetic dyes.
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GelatinNo checked product
No checked Sodium Oxybate product lists gelatin.
Find a version without it
Every current Sodium Oxybate product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Alkermes, Inc. 5 products | ||
| 4.5 g extended-release oral suspensionNDC 13551-0001-07 | No inactive-ingredient list on the label | No list we could read |
| 6 g extended-release oral suspensionNDC 13551-0002-07 | No inactive-ingredient list on the label | No list we could read |
| 7.5 g extended-release oral suspensionNDC 13551-0003-07 | No inactive-ingredient list on the label | No list we could read |
| 9 g extended-release oral suspensionNDC 13551-0004-07 | No inactive-ingredient list on the label | No list we could read |
| kitsNDC 13551-0005-01 | No current label | Not available |
| Amneal Pharmaceuticals LLC 1 product | ||
| 500 mg/mL oral solutionNDC 65162-0065-87 | None of these listed |
Show 4 ingredientsMALIC ACID, SODIUM HYDROXIDE, SODIUM PROPYLPARABEN, WATER |
| Camber Pharmaceuticals, Inc. 1 product | ||
| 0.5 g/mL oral solutionNDC 31722-0891-18 | None of these listed |
Show 2 ingredientsMALIC ACID, WATER |
| Hikma Pharmaceuticals USA Inc. 1 product | ||
| 0.5 g/mL oral solutionNDC 00054-9628-57 | No inactive-ingredient list on the label | No list we could read |
| Jazz Pharmaceuticals, Inc. 1 product | ||
| 0.5 g/mL oral solutionNDC 68727-0100-01 | No inactive-ingredient list on the label | No list we could read |
| XLCare Pharmaceuticals, Inc. 1 product | ||
| 0.5 g/mL oral solutionNDC 72865-0349-18 | None of these listed |
Show 2 ingredientsMALIC ACID, WATER |
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.
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 Sodium Oxybate inactive ingredients
Is Sodium Oxybate gluten-free?
Does Sodium Oxybate contain lactose?
Does Sodium Oxybate contain soy?
Is there a dye-free Sodium Oxybate?
Does Sodium Oxybate 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 Sodium Oxybate 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 Sodium Oxybate guide