Formoterol Oral Inhalation inactive ingredients by manufacturer
Wondering whether your Formoterol Oral Inhalation 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 Formoterol Oral Inhalation 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 12 of the 14 current Formoterol Oral Inhalation products on the market today, from 13 companies listing it with the FDA, and lined them up side by side. 2 are still being read and will appear on a later visit.
Ask about your bottle
Is there something in your Formoterol Oral Inhalation? 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 Formoterol Oral Inhalation products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Formoterol Oral Inhalation product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Formoterol Oral Inhalation product lists a wheat or gluten source.
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SoyNo checked product
No checked Formoterol Oral Inhalation product lists soy.
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Synthetic dyesNo checked product
No checked Formoterol Oral Inhalation product lists synthetic dyes.
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GelatinNo checked product
No checked Formoterol Oral Inhalation product lists gelatin.
Find a version without it
Every current Formoterol Oral Inhalation product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Alembic Pharmaceuticals Inc. 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 62332-0655-30 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| Bryant Ranch Prepack 2 products | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 63629-8814-01 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM CITRATE, UNSPECIFIED FORM, WATER |
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 63629-8813-01 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM CITRATE, UNSPECIFIED FORM, WATER |
| Devatis, Inc. 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 73043-0051-93 | None of these listed |
Show 3 ingredientsCITRIC ACID, SODIUM CHLORIDE, SODIUM CITRATE |
| Dr. Reddy's Laboratories Inc. 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 43598-0778-30 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| Ingenus Pharmaceuticals, LLC 1 product | ||
| 0.02 mg/2 mL inhalation solution (nebulizer)NDC 50742-0394-30 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM CITRATE, UNSPECIFIED FORM, WATER |
| Lifestar Pharma LLC 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 70756-0608-60 | Still being read | Not read yet |
| Lupin Pharmaceuticals, Inc. 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 70748-0261-30 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| Micro Labs Limited 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 42571-0463-62 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| Mylan Pharmaceuticals Inc. 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 00378-1631-91 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| NorthStar RxLLC 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 72603-0620-30 | Still being read | Not read yet |
| Ritedose Pharmaceuticals, LLC 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 76204-0030-01 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| Teva Pharmaceuticals USA, Inc. 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 00093-4061-06 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM CITRATE, UNSPECIFIED FORM, WATER |
| Viatris Specialty LLC 1 product | ||
| 20 mcg/2 mL inhalation solution (nebulizer)NDC 49502-0605-05 | None of these listed |
Show 4 ingredientsCITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, TRISODIUM CITRATE DIHYDRATE, 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 Formoterol Oral Inhalation inactive ingredients
Is Formoterol Oral Inhalation gluten-free?
Does Formoterol Oral Inhalation contain lactose?
Does Formoterol Oral Inhalation contain soy?
Is there a dye-free Formoterol Oral Inhalation?
Does Formoterol Oral Inhalation 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 Formoterol Oral Inhalation 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 Formoterol Oral Inhalation guide