Inactive ingredients by manufacturer

Zoledronic Acid inactive ingredients by manufacturer

Wondering whether your Zoledronic Acid 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 Zoledronic Acid 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 31 of the 35 current Zoledronic Acid products on the market today, from 22 companies listing it with the FDA, and lined them up side by side. 4 are still being read and will appear on a later visit.

Ask about your bottle

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

  1. LactoseNo checked product

    No checked Zoledronic Acid product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Zoledronic Acid product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Zoledronic Acid product lists soy.

  4. Synthetic dyesNo checked product

    No checked Zoledronic Acid product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Zoledronic Acid product lists gelatin.

Also listed by some products: Sorbitol or mannitol 31 of 31

Find a version without it

Every current Zoledronic Acid product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
Accord Healthcare Inc. 1 product
4 mg/5 mL injectionNDC 16729-0242-31 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
AuroMedics Pharma LLC 1 product
4 mg/5 mL injectionNDC 55150-0266-05 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, UNSPECIFIED FORM, WATER
Avenacy Inc. 1 product
4 mg/5 mL injectionNDC 83634-0801-05 Sorbitol or mannitol
Show 3 ingredients

mannitol, sodium citrate, water
BluePoint Laboratories 3 products
4 mg/5 mL injectionNDC 68001-0437-25 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, UNSPECIFIED FORM, WATER
4 mg/5 mL injectionNDC 68001-0610-25 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
5 mg/100 mL injectionNDC 68001-0611-33 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
BPI Labs LLC 2 products
4 mg/5 mL injectionNDC 54288-0183-01 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
4 mg/5 mL injectionNDC 54288-0100-01 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
Dr. Reddy's Laboratories Inc 1 product
4 mg/100 mL injectionNDC 43598-0255-52 Still being read Not read yet
Dr.Reddy's Laboratories Inc 1 product
5 mg/100 mL injectionNDC 43598-0331-11 Still being read Not read yet
Dr. Reddy's Laboratories Inc. 2 products
4 mg/5 mL injectionNDC 43598-0233-11 Sorbitol or mannitol
Show 3 ingredients

Mannitol, Sodium Citrate, Water
4 mg/5 mL injectionNDC 43598-0330-11 Sorbitol or mannitol
Show 3 ingredients

Mannitol, Sodium Citrate, Water
Dr. Reddy's Laboratories Limited 1 product
4 mg/5 mL injectionNDC 55111-0685-07 Still being read Not read yet
Dr.Reddy's Laboratories Ltd 1 product
5 mg/100 mL injectionNDC 55111-0688-52 Sorbitol or mannitol
Show 3 ingredients

Mannitol, Sodium Citrate, Water
Eugia US LLC 1 product
5 mg/100 mL injectionNDC 55150-0283-99 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, TRISODIUM CITRATE DIHYDRATE, WATER
Fosun Pharma Usa Inc 1 product
5 mg/100 mL injectionNDC 72266-0152-01 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
Fresenius Kabi USA, LLC 2 products
4 mg/5 mL injectionNDC 63323-0961-98 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
5 mg/100 mL injectionNDC 63323-0966-00 Sorbitol or mannitol
Show 2 ingredients

MANNITOL, SODIUM CITRATE
Gland Pharma Limited 6 products
0.04 mg/mL injectionNDC 68083-0672-01 Still being read Not read yet
4 mg/5 mL injectionNDC 68083-0615-01 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
4 mg/5 mL injectionNDC 68083-0116-01 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
4 mg/100 mL injectionNDC 68083-0142-01 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
5 mg/100 mL injectionNDC 68083-0256-01 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
5 mg/100 mL injectionNDC 68083-0135-01 Sorbitol or mannitol
Show 2 ingredients

Mannitol, Sodium Citrate
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 1 product
4 mg/5 mL injectionNDC 23155-0170-31 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
Hikma Pharmaceuticals USA Inc. 1 product
4 mg/5 mL injectionNDC 00143-9642-01 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
Meitheal Pharmaceuticals Inc. 1 product
5 mg/100 mL injectionNDC 71288-0806-51 Sorbitol or mannitol
Show 3 ingredients

mannitol, sodium citrate, water
Mylan Institutional LLC 3 products
4 mg/5 mL injectionNDC 67457-0390-54 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, UNSPECIFIED FORM, WATER
5 mg/100 mL injectionNDC 67457-0794-10 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, UNSPECIFIED FORM, WATER
5 mg/100 mL injectionNDC 67457-0619-10 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, UNSPECIFIED FORM, WATER
Northstar Rx Llc 1 product
4 mg/5 mL injectionNDC 72603-0198-01 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, WATER
Sagent Pharmaceuticals 2 products
0.04 mg/mL injectionNDC 25021-0826-67 Sorbitol or mannitol
Show 4 ingredients

mannitol, sodium chloride, sodium citrate, water
0.05 mg/mL injectionNDC 25021-0830-82 Sorbitol or mannitol
Show 3 ingredients

mannitol, sodium citrate, water
Sandoz Inc 1 product
5 mg/100 mL injectionNDC 66758-0155-46 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, UNSPECIFIED FORM, WATER
Westminster Pharmaceuticals, LLC 1 product
4 mg/5 mL injectionNDC 69367-0190-50 Sorbitol or mannitol
Show 3 ingredients

MANNITOL, SODIUM CITRATE, UNSPECIFIED FORM, 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.

Zoledronic Acid and sorbitol or mannitol

Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. Every checked Zoledronic Acid product (31) lists sorbitol or mannitol.

Lists sorbitol or mannitol

At the pharmacy counter

How to use this at the pharmacy counter

  1. 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.
  2. 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.
  3. 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.
  4. 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 Zoledronic Acid product suits you →

Common questions about Zoledronic Acid inactive ingredients

Is Zoledronic Acid gluten-free?
This page cannot certify any Zoledronic Acid product gluten-free; it reports what each label declares. Of the 31 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 Zoledronic Acid contain lactose?
No checked Zoledronic Acid 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 Zoledronic Acid contain soy?
No checked Zoledronic Acid 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 Zoledronic Acid?
No checked Zoledronic Acid 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 Zoledronic Acid contain gelatin?
No checked Zoledronic Acid 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 September 25, 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 Zoledronic Acid products in the FDA's current NDC directory (openFDA), as of September 25, 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 Zoledronic Acid guide