Succinylcholine inactive ingredients by manufacturer
Wondering whether your Succinylcholine 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 Succinylcholine 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 34 of the 38 current Succinylcholine products on the market today, from 28 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 could not be linked to a current label.
Ask about your bottle
Is there something in your Succinylcholine? 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 Succinylcholine products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Succinylcholine product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Succinylcholine product lists a wheat or gluten source.
-
SoyNo checked product
No checked Succinylcholine product lists soy.
-
Synthetic dyesNo checked product
No checked Succinylcholine product lists synthetic dyes.
-
GelatinNo checked product
No checked Succinylcholine product lists gelatin.
Find a version without it
Every current Succinylcholine product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Amring Pharmaceuticals Inc. 1 product | ||
| 20 mg/mL injectionNDC 69918-0700-10 | No current label | Not available |
| Baxter Healthcare Corporation 2 products | ||
| 20 mg/mL injectionNDC 43066-0129-05 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 43066-0127-05 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| BE Pharmaceuticals Inc. 1 product | ||
| 20 mg/mL injectionNDC 71839-0121-25 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Camber Pharmaceuticals, Inc. 1 product | ||
| 20 mg/mL injectionNDC 31722-0981-31 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Civica, Inc. 1 product | ||
| 20 mg/mL injectionNDC 72572-0750-10 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Devatis, Inc. 1 product | ||
| 20 mg/mL injectionNDC 73043-0021-01 | None of these listed |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Dr.Reddy's Laboratories Inc., 1 product | ||
| 20 mg/mL injectionNDC 43598-0666-25 | None of these listed |
Show 5 ingredientsHydrochloric Acid, Methylparaben, Propylparaben, SODIUM CHLORIDE, Sodium Hydroxide |
| Eugia US LLC 1 product | ||
| 20 mg/mL injectionNDC 55150-0315-25 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Fresenius Kabi USA, LLC 1 product | ||
| 20 mg/mL injectionNDC 63323-0943-10 | None of these listed |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Fresenius Kabi USA LLC 2 products | ||
| 20 mg/mL injectionNDC 65219-0274-05 | None of these listed |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| 20 mg/mL injectionNDC 65219-0276-10 | None of these listed |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Gland Pharma Limited 1 product | ||
| 20 mg/mL injectionNDC 68083-0450-25 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Henry Schein, Inc. 1 product | ||
| 20 mg/mL injectionNDC 00404-9983-20 | Still being read | Not read yet |
| HF Acquisition Co LLC, DBA HealthFirst 1 product | ||
| 20 mg/mL injectionNDC 51662-1525-01 | None of these listed |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORITE, SODIUM HYDROXIDE |
| Hikma Pharmaceuticals USA Inc. 1 product | ||
| 20 mg/mL injectionNDC 00143-9338-25 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Hospira, Inc. 1 product | ||
| 20 mg/mL injectionNDC 00409-6629-02 | None of these listed |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Indoco Remedies Limited 1 product | ||
| 20 mg/mL injectionNDC 14445-0407-25 | None of these listed |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Lifestar Pharma LLC 1 product | ||
| 20 mg/mL injectionNDC 70756-0613-10 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Medical Purchasing Solutions, LLC 7 products | ||
| 20 mg/mL injectionNDC 71872-7275-01 | None of these listed |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| 20 mg/mL injectionNDC 71872-7279-01 | Still being read | Not read yet |
| 20 mg/mL injectionNDC 71872-7166-01 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 71872-7272-01 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 71872-7241-01 | Still being read | Not read yet |
| 20 mg/mL injectionNDC 71872-7167-01 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 71872-7221-01 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Meitheal Pharmaceuticals Inc. 1 product | ||
| 20 mg/mL injectionNDC 71288-0719-11 | None of these listed |
Show 6 ingredientshydrochloric acid, methylparaben, propylparaben, sodium chloride, sodium hydroxide, water |
| Micro Labs Limited 1 product | ||
| 200 mg/10 mL injectionNDC 42571-0371-87 | None of these listed |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Piramal Critical Care Inc 1 product | ||
| 20 mg/mL injectionNDC 66794-0232-42 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| ProPharma Distribution 1 product | ||
| 20 mg/mL injectionNDC 84549-0301-25 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Remedyrepack Inc. 1 product | ||
| 20 mg/mL injectionNDC 70518-4409-00 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Sandoz Inc 2 products | ||
| 20 mg/mL injectionNDC 00781-3411-95 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| 20 mg/mL injectionNDC 00781-9053-95 | None of these listed |
Show 4 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Somerset Therapeutics, LLC 2 products | ||
| 20 mg/mL injectionNDC 70069-0783-10 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| 20 mg/mL injectionNDC 70069-0301-10 | None of these listed |
Show 6 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER |
| Steriscience Specialties Private Limited 1 product | ||
| 20 mg/mL injectionNDC 82449-0232-02 | None of these listed |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Zydus Pharmaceuticals USA Inc. 1 product | ||
| 20 mg/mL injectionNDC 70710-1377-02 | None of these listed |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE |
| Zydus Lifesciences Limited 1 product | ||
| 20 mg/mL injectionNDC 70771-1352-07 | None of these listed |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, 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.
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 Succinylcholine inactive ingredients
Is Succinylcholine gluten-free?
Does Succinylcholine contain lactose?
Does Succinylcholine contain soy?
Is there a dye-free Succinylcholine?
Does Succinylcholine 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 Succinylcholine 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 Succinylcholine guide