Dobutamine inactive ingredients by manufacturer
Wondering whether your Dobutamine 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 Dobutamine 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 13 of the 14 current Dobutamine products on the market today, from 6 companies listing it with the FDA, and lined them up side by side. 1 is still being read and will appear on a later visit.
Ask about your bottle
Is there something in your Dobutamine? 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 Dobutamine products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Dobutamine product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Dobutamine product lists a wheat or gluten source.
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SoyNo checked product
No checked Dobutamine product lists soy.
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Synthetic dyesNo checked product
No checked Dobutamine product lists synthetic dyes.
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GelatinNo checked product
No checked Dobutamine product lists gelatin.
Also listed by some products: Sulfites 13 of 13 Sugar 9 of 13
Find a version without it
Every current Dobutamine product and what its label lists
Dobutamine 12.5 mg/mL injection 3 companies Sulfites 3
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| HF Acquisition Co LLC, DBA HealthFirstNDC 51662-1337-01 | Sulfites |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM METABISULFITE |
| HikmaNDC 00143-9141-10 | Sulfites |
Show 4 ingredientsHYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| HospiraNDC 00409-2344-01 | Sulfites |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM METABISULFITE |
Dobutamine 100 mg/100 mL injection 5 companies Sulfites 5 Sugar (sucrose, dextrose) 5
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Baxter HealthcareNDC 00338-1073-02 | Sulfites Sugar (sucrose, dextrose) |
Show 5 ingredientsDEXTROSE MONOHYDRATE, HYDROCHLORIC ACID, SODIUM BISULFITE, SODIUM HYDROXIDE, WATER |
| HF Acquisition Co. LLC, DBA HealthFirstNDC 51662-1664-01 | Sulfites Sugar (sucrose, dextrose) |
Show 6 ingredientsDEXTROSE MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| HF Acquisition Co LLC, DBA HealthFirstNDC 51662-1566-01 | Sulfites Sugar (sucrose, dextrose) |
Show 5 ingredientsDEXTROSE MONOHYDRATE, HYDROCHLORIC ACID, SODIUM BISULFITE, SODIUM HYDROXIDE, WATER |
| HF Acquisition Co LLC, DBA HealthFirstNDC 51662-1697-01 | Sulfites Sugar (sucrose, dextrose) |
Show 6 ingredientsDEXTROSE MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| HospiraNDC 00409-0025-10 | Sulfites Sugar (sucrose, dextrose) |
Show 6 ingredientsDEXTROSE MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
Dobutamine 200 mg/100 mL injection 3 companies Sulfites 3 Sugar (sucrose, dextrose) 3
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Baxter HealthcareNDC 00338-1075-02 | Sulfites Sugar (sucrose, dextrose) |
Show 5 ingredientsDEXTROSE MONOHYDRATE, HYDROCHLORIC ACID, SODIUM BISULFITE, SODIUM HYDROXIDE, WATER |
| HF Acquisition Co LLC, DBA HealthFirstNDC 51662-1705-01 | Sulfites Sugar (sucrose, dextrose) |
Show 6 ingredientsDEXTROSE MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
| HospiraNDC 00409-0151-10 | Sulfites Sugar (sucrose, dextrose) |
Show 6 ingredientsDEXTROSE MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM METABISULFITE, WATER |
Dobutamine 250 mg/20 mL injection 1 company Sulfites 1
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Slate RunNDC 70436-0203-80 | Sulfites |
Show 3 ingredientsHYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM METABISULFITE |
Dobutamine 400 mg/100 mL injection 2 companies Sulfites 1 Sugar (sucrose, dextrose) 1
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Baxter HealthcareNDC 00338-1077-02 | Still being read | Not read yet |
| HospiraNDC 00409-1100-10 | Sulfites Sugar (sucrose, dextrose) |
Show 6 ingredientsDEXTROSE MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, 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.
Dobutamine and sulfites
Sulfites: metabisulfite or bisulfite preservatives; a concern with sulfite sensitivity or asthma. Every checked Dobutamine product (13) lists sulfites.
Show which Dobutamine products list sulfites and which do not, by product and company
Lists sulfites
- 12.5 mg/mL injection: HF Acquisition Co LLC, DBA HealthFirst, Hikma, Hospira
- 100 mg/100 mL injection: Baxter Healthcare, HF Acquisition Co. LLC, DBA HealthFirst, HF Acquisition Co LLC, DBA HealthFirst, HF Acquisition Co LLC, DBA HealthFirst, Hospira
- 200 mg/100 mL injection: Baxter Healthcare, HF Acquisition Co LLC, DBA HealthFirst, Hospira
- 250 mg/20 mL injection: Slate Run
- 400 mg/100 mL injection: Hospira
Dobutamine without sugar (sucrose or dextrose)
Sugar (sucrose, dextrose): A consideration in diabetes, mostly in liquids and chewables. 9 of 13 checked products list sugar (sucrose or dextrose); 4 do not.
Show which Dobutamine products list sugar (sucrose or dextrose) and which do not, by product and company
Does not list sugar (sucrose or dextrose)
- 12.5 mg/mL injection: HF Acquisition Co LLC, DBA HealthFirst, Hikma, Hospira
- 250 mg/20 mL injection: Slate Run
Lists sugar (sucrose or dextrose)
- 100 mg/100 mL injection: Baxter Healthcare, HF Acquisition Co. LLC, DBA HealthFirst, HF Acquisition Co LLC, DBA HealthFirst, HF Acquisition Co LLC, DBA HealthFirst, Hospira
- 200 mg/100 mL injection: Baxter Healthcare, HF Acquisition Co LLC, DBA HealthFirst, Hospira
- 400 mg/100 mL injection: Hospira
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 Dobutamine inactive ingredients
Is Dobutamine gluten-free?
Does Dobutamine contain lactose?
Does Dobutamine contain soy?
Is there a dye-free Dobutamine?
Does Dobutamine 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 Dobutamine 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 Dobutamine guide