Gentamicin Injection inactive ingredients by manufacturer

Name: Gentamicin Injection Inactive Ingredients by Manufacturer
Creator: HelloPharmacist

Wondering whether your Gentamicin Injection 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 Gentamicin Injection 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 21 of the 22 current Gentamicin Injection products on the market today, from 11 companies listing it with the FDA, and lined them up side by side. 1 label has no inactive-ingredient list we could read, so that product cannot be compared.

Ask about your bottle

Is there something in your Gentamicin Injection? 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 Gentamicin Injection products list lactose, a gluten source, soy, dyes or gelatin?

LactoseNo checked product

No checked Gentamicin Injection product lists lactose.
Wheat or gluten sourceNo checked product

No checked Gentamicin Injection product lists a wheat or gluten source.
SoyNo checked product

No checked Gentamicin Injection product lists soy.
Synthetic dyesNo checked product

No checked Gentamicin Injection product lists synthetic dyes.
GelatinNo checked product

No checked Gentamicin Injection product lists gelatin.

Also listed by some products: Sulfites 13 of 21

Find a version without it

Every current Gentamicin Injection product and what its label lists

Hide products that list:

Product	Lists	Inactive ingredients on the label
Baxter Healthcare Corporation 5 products
60 mg/50 mL injectionNDC 00338-0507-41	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
80 mg/50 mL injectionNDC 00338-0509-41	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
80 mg/100 mL injectionNDC 00338-0503-48	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
100 mg/50 mL injectionNDC 00338-0511-41	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
100 mg/100 mL injectionNDC 00338-0505-48	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Cardinal Health 107, LLC 1 product
40 mg/mL injectionNDC 55154-2392-05	Sulfites	Show 5 ingredients EDETATE DISODIUM ANHYDROUS, METHYLPARABEN, PROPYLPARABEN, SODIUM METABISULFITE, WATER
Eugia US LLC 3 products
10 mg/mL injectionNDC 55150-0401-25	None of these listed	Show 3 ingredients SODIUM HYDROXIDE, SULFURIC ACID, WATER
40 mg/mL injectionNDC 55150-0403-25	Sulfites	Show 7 ingredients EDETATE DISODIUM, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER
40 mg/mL injectionNDC 55150-0402-25	Sulfites	Show 7 ingredients EDETATE DISODIUM, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER
Fresenius Kabi USA, LLC 2 products
10 mg/mL injectionNDC 63323-0173-02	None of these listed	Show 3 ingredients SODIUM HYDROXIDE, SULFURIC ACID, WATER
40 mg/mL injectionNDC 63323-0010-02	Sulfites	Show 7 ingredients EDETATE DISODIUM, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER
Henry Schein, Inc 1 product
40 mg/mL injectionNDC 00404-9866-20	None of these listed	Show 2 ingredients SODIUM HYDROXIDE, SULFURIC ACID
Henry Schein, Inc. 1 product
40 mg/mL injectionNDC 00404-9865-02	No inactive-ingredient list on the label	No list we could read
HF Acquisition Co LLC, DBA HealthFirst 2 products
40 mg/mL injectionNDC 51662-1508-03	Sulfites	Show 6 ingredients EDETATE DISODIUM, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID
40 mg/mL injectionNDC 51662-1597-03	Sulfites	Show 7 ingredients EDETATE DISODIUM ANHYDROUS, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER
Hikma Pharmaceuticals USA Inc. 2 products
40 mg/mL injectionNDC 00143-9128-25	Sulfites	Show 6 ingredients EDETATE DISODIUM, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID
40 mg/mL injectionNDC 00143-9129-10	Sulfites	Show 6 ingredients EDETATE DISODIUM, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID
Hospira, Inc. 1 product
40 mg/mL injectionNDC 00409-1207-03	Sulfites	Show 7 ingredients EDETATE DISODIUM ANHYDROUS, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER
Medical Purchasing Solutions, LLC 3 products
40 mg/mL injectionNDC 71872-7216-01	Sulfites	Show 7 ingredients EDETATE DISODIUM ANHYDROUS, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER
40 mg/mL injectionNDC 71872-7311-01	Sulfites	Show 7 ingredients EDETATE DISODIUM, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER
40 mg/mL injectionNDC 71872-7337-01	Sulfites	Show 7 ingredients EDETATE DISODIUM ANHYDROUS, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER
Remedyrepack Inc. 1 product
40 mg/mL injectionNDC 70518-4757-00	Sulfites	Show 7 ingredients EDETATE DISODIUM, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC 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.

Gentamicin Injection without sulfites

Sulfites: metabisulfite or bisulfite preservatives; a concern with sulfite sensitivity or asthma. 13 of 21 checked products list sulfites; 8 do not.

Does not list sulfites

Baxter Healthcare: 60 mg/50 mL injection, 80 mg/50 mL injection, 80 mg/100 mL injection, 100 mg/50 mL injection, 100 mg/100 mL injection
Eugia: 10 mg/mL injection
Fresenius Kabi: 10 mg/mL injection
Henry Schein, Inc: 40 mg/mL injection

Lists sulfites

Cardinal Health 107: 40 mg/mL injection
Eugia: 40 mg/mL injection (NDC 55150-0403-25), 40 mg/mL injection (NDC 55150-0402-25)
Fresenius Kabi: 40 mg/mL injection
HF Acquisition Co LLC, DBA HealthFirst: 40 mg/mL injection (NDC 51662-1508-03), 40 mg/mL injection (NDC 51662-1597-03)
Hikma: 40 mg/mL injection (NDC 00143-9128-25), 40 mg/mL injection (NDC 00143-9129-10)
Hospira: 40 mg/mL injection
Medical Purchasing Solutions: 40 mg/mL injection (NDC 71872-7216-01), 40 mg/mL injection (NDC 71872-7311-01), 40 mg/mL injection (NDC 71872-7337-01)
Remedyrepack: 40 mg/mL injection

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.

Ask Dr. Staiger which Gentamicin Injection product suits you →

Common questions about Gentamicin Injection inactive ingredients

Is Gentamicin Injection gluten-free?

This page cannot certify any Gentamicin Injection product gluten-free; it reports what each label declares. Of the 21 products checked, none lists a wheat, barley, rye or gluten ingredient, and none lists a starch without a stated source. If you have celiac disease, ask the manufacturer's medical information line for a written gluten statement for the lot you have.

Does Gentamicin Injection contain lactose?

No checked Gentamicin Injection product lists lactose on its label. People with a milk allergy or a strong intolerance often prefer a version that does not list it.

Does Gentamicin Injection contain soy?

No checked Gentamicin Injection product lists a soy ingredient (soybean oil or soy lecithin) on its label. Soy lecithin is the usual form and the amount is small, but people with a soy allergy often prefer a version that does not list it.

Is there a dye-free Gentamicin Injection?

No checked Gentamicin Injection product lists a synthetic dye (an FD&C or D&C colorant) on its label. Colorants often differ by strength within one company's line, so compare the lists above strength by strength.

Does Gentamicin Injection contain gelatin?

No checked Gentamicin Injection product lists gelatin on its label. Gelatin is usually bovine or porcine and the label rarely says which; for kosher, halal or vegetarian needs, ask the manufacturer.

Why do the inactive ingredients differ between manufacturers?

A generic must match the brand's active ingredient, strength and dose form. For injectable, ophthalmic and otic products the FDA generally requires the inactive ingredients to match the reference product as well, so the lists on this page differ less than they do for tablets and capsules; the differences that remain come from the exact product and container each company files.

Can my pharmacy give me a specific manufacturer's version?

Often, if you ask before the prescription is filled: many pharmacies order from wholesalers that carry several companies' versions and can request a particular one. Some pharmacies buy a generic from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check. Give them the NDC from this page; the company name alone is often enough.

How current is this list?

The products are the ones in the FDA's current NDC directory as of October 6, 2026, and each inactive-ingredient list is the manufacturer's FDA label as our label sync last read it. Formulations change, so check the label on your own bottle and ask your pharmacist if a refill looks different.

Sources: the products are the finished Gentamicin Injection 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 Gentamicin Injection guide