Procainamide inactive ingredients by manufacturer
Wondering whether your Procainamide 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 Procainamide 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 16 current Procainamide products on the market today, from 11 companies listing it with the FDA, and lined them up side by side.
Ask about your bottle
Is there something in your Procainamide? 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.
Check your bottle
Let's take a closer look at your Procainamide.
Pick your bottle and tap what you want to check. The answer comes from that product's own FDA label, which is already on this page.
1 Which bottle do you have?
Or tap your way to it: the form, then the strength, then the company.
2 What do you want to check?
Nothing tapped? We check the five big ones.
Pick your bottle to read its label, or tap an ingredient to see which Procainamide products leave it out.
At a glance
Which Procainamide products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Procainamide product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Procainamide product lists a wheat or gluten source.
-
SoyNo checked product
No checked Procainamide product lists soy.
-
Synthetic dyesNo checked product
No checked Procainamide product lists synthetic dyes.
-
GelatinNo checked product
No checked Procainamide product lists gelatin.
Also listed by some products: Sulfites 16 of 16 Benzyl alcohol 4 of 16
Find a version without it
Every current Procainamide product and what its label lists
Fastest way: search by NDC. It is printed on your bottle's pharmacy label. If it is not, call your pharmacy: they have it on record.
An NDC (National Drug Code) is the FDA's number for one exact product from one company in one package size, written like 60505-0121-01: the first part is the company, the middle the product and strength, the last the package size. Codes that differ only in the last part are the same product in different pack sizes and share one label, so any of them finds the right product here. Two bottles of the same medicine from different companies can have different inactive ingredients, which is why the pharmacy needs the number, not just the name.
Procainamide 100 mg/mL injection 12 companies Sulfites 12 Benzyl alcohol 4
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Caplin SterilesNDC 65145-0155-10 | Sulfites |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| GlandNDC 68083-0603-25 | Sulfites |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| HF Acquisition Co LLC, DBA HealthFirstNDC 51662-1334-01 Other pack sizes, same label: 51662-1334-03 | Sulfites |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| HF Acquisition Co LLC, DBA HealthFirstNDC 51662-1630-03 | Sulfites Benzyl alcohol |
Show 4 ingredientsBENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM BISULFITE, SODIUM HYDROXIDE |
| HospiraNDC 00409-1902-01 | Sulfites |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| International Medication SystemsNDC 76329-3399-05 | Sulfites Benzyl alcohol |
Show 4 ingredientsBENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM BISULFITE, SODIUM HYDROXIDE |
| Medical Purchasing Solutions, LLCNDC 71872-7113-01 | Sulfites |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| Medical Purchasing Solutions, LLC.NDC 71872-7353-01 | Sulfites |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| NexusNDC 14789-0901-10 | Sulfites |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| ProPharma DistributionNDC 84549-0399-05 | Sulfites Benzyl alcohol |
Show 4 ingredientsBENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM BISULFITE, SODIUM HYDROXIDE |
| RemedyrepackNDC 70518-4208-00 | Sulfites Benzyl alcohol |
Show 4 ingredientsBENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM BISULFITE, SODIUM HYDROXIDE |
| SagentNDC 25021-0322-10 | Sulfites |
Show 5 ingredientsHydrochloric Acid, Methylparaben, Sodium Hydroxide, Sodium Metabisulfite, Water |
Procainamide 500 mg/mL injection 4 companies Sulfites 4
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Caplin SterilesNDC 65145-0156-10 | Sulfites |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| GlandNDC 68083-0604-25 | Sulfites |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| NexusNDC 14789-0900-02 | Sulfites |
Show 5 ingredientsHYDROCHLORIC ACID, METHYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| SagentNDC 25021-0323-02 | Sulfites |
Show 5 ingredientsHydrochloric Acid, Methylparaben, Sodium Hydroxide, Sodium Metabisulfite, 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.
Procainamide and sulfites
Sulfites: metabisulfite or bisulfite preservatives; a concern with sulfite sensitivity or asthma. Every checked Procainamide product (16) lists sulfites.
Show which Procainamide products list sulfites and which do not, by product and company
Lists sulfites
- 100 mg/mL injection: Caplin Steriles, Gland, HF Acquisition Co LLC, DBA HealthFirst, HF Acquisition Co LLC, DBA HealthFirst, Hospira, International Medication Systems, Medical Purchasing Solutions, LLC, Medical Purchasing Solutions, LLC., Nexus, ProPharma Distribution, Remedyrepack, Sagent
- 500 mg/mL injection: Caplin Steriles, Gland, Nexus, Sagent
Procainamide without benzyl alcohol
Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 4 of 16 checked products list benzyl alcohol; 12 do not.
Show which Procainamide products list benzyl alcohol and which do not, by product and company
Does not list benzyl alcohol
- 100 mg/mL injection: Caplin Steriles, Gland, HF Acquisition Co LLC, DBA HealthFirst, Hospira, Medical Purchasing Solutions, LLC, Medical Purchasing Solutions, LLC., Nexus, Sagent
- 500 mg/mL injection: Caplin Steriles, Gland, Nexus, Sagent
Lists benzyl alcohol
- 100 mg/mL injection: HF Acquisition Co LLC, DBA HealthFirst, International Medication Systems, ProPharma Distribution, Remedyrepack
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 Procainamide inactive ingredients
Is Procainamide gluten-free?
Does Procainamide contain lactose?
Does Procainamide contain soy?
Is there a dye-free Procainamide?
Does Procainamide contain gelatin?
Why do the inactive ingredients differ between manufacturers?
Who decides what counts as a gluten source, a dye or soy on this page?
The NDC on my bottle ends differently from the one on this page. Is it the same product?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Procainamide 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 Procainamide guide