Inactive ingredients by manufacturer

Daptomycin inactive ingredients by manufacturer

Wondering whether your Daptomycin 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 Daptomycin 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 44 of the 47 current Daptomycin products on the market today, from 27 companies listing it with the FDA, and lined them up side by side. 3 labels have no inactive-ingredient list we could read, so those products cannot be compared.

Ask about your bottle

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

  1. LactoseNo checked product

    No checked Daptomycin product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Daptomycin product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Daptomycin product lists soy.

  4. Synthetic dyesNo checked product

    No checked Daptomycin product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Daptomycin product lists gelatin.

Also listed by some products: Sorbitol or mannitol 1 of 44 Sugar 1 of 44

Find a version without it

Every current Daptomycin product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
Accord Healthcare, Inc. 1 product
350 mg/7 mL injectionNDC 16729-0434-05 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Accord Healthcare Inc. 1 product
500 mg/10 mL injectionNDC 16729-0435-05 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Apotex Corp. 1 product
500 mg/10 mL injectionNDC 60505-6229-04 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Aspiro Pharma Limited 1 product
500 mg/10 mL injectionNDC 72201-1009-00 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Baxter Healthcare Corporation 5 products
350 mg/50 mL injectionNDC 00338-0712-24 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, WATER
500 mg/10 mL injectionNDC 60977-0145-01 Sorbitol or mannitol
Show 4 ingredients

HYDROCHLORIC ACID, MANNITOL, SODIUM HYDROXIDE, SORBITOL
500 mg/50 mL injectionNDC 00338-0714-24 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, WATER
700 mg/100 mL injectionNDC 00338-0716-12 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, WATER
1000 mg/100 mL injectionNDC 00338-0718-12 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, WATER
BE Pharmaceuticals Inc. 2 products
350 mg/7 mL injectionNDC 71839-0108-01 None of these listed
Show 2 ingredients

SODIUM HYDROXIDE, WATER
500 mg/10 mL injectionNDC 71839-0107-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Biocon Pharma Inc. 1 product
500 mg/10 mL injectionNDC 70377-0093-91 None of these listed
Show 2 ingredients

NITROGEN, Sodium Hydroxide
BluePoint Laboratories 1 product
500 mg/10 mL injectionNDC 68001-0376-68 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Camber Pharmaceuticals, Inc. 2 products
350 mg/7 mL injectionNDC 31722-0215-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
500 mg/10 mL injectionNDC 31722-0216-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Civica, Inc. 3 products
350 mg/7 mL injectionNDC 72572-0100-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
500 mg/10 mL injectionNDC 72572-0102-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
500 mg/10 mL injectionNDC 72572-0158-01 None of these listed
Show 4 ingredients

ARGININE, HISTIDINE, HYDROCHLORIC ACID, ISOLEUCINE
Dr. Reddy's Laboratories Inc., 1 product
350 mg/7 mL injectionNDC 43598-0476-11 None of these listed
Show 1 ingredient

Sodium Hydroxide
Dr.Reddy's Laboratories Inc., 1 product
500 mg/10 mL injectionNDC 43598-0413-11 None of these listed
Show 1 ingredient

Sodium Hydroxide
Eugia US LLC 1 product
500 mg/10 mL injectionNDC 55150-0344-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Fresenius Kabi USA, LLC 1 product
500 mg/10 mL injectionNDC 63323-0371-10 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Hainan Poly Pharm., Co., Ltd. 1 product
500 mg/20 mL injectionNDC 14335-0120-01 No inactive-ingredient list on the label No list we could read
Hikma Pharmaceuticals USA Inc. 5 products
350 mg/7 mL injectionNDC 00143-9455-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
350 mg/7 mL injectionNDC 00143-9456-01 None of these listed
Show 4 ingredients

ARGININE, HISTIDINE, HYDROCHLORIC ACID, ISOLEUCINE
500 mg/10 mL injectionNDC 00143-9444-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
500 mg/10 mL injectionNDC 00143-9445-01 None of these listed
Show 4 ingredients

ARGININE, HISTIDINE, HYDROCHLORIC ACID, ISOLEUCINE
500 mg/10 mL injectionNDC 00143-9465-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Hospira, Inc. 2 products
350 mg/7 mL injectionNDC 00409-0120-01 None of these listed
Show 2 ingredients

ANHYDROUS CITRIC ACID, SODIUM HYDROXIDE
500 mg/10 mL injectionNDC 00409-0122-01 None of these listed
Show 2 ingredients

ANHYDROUS CITRIC ACID, SODIUM HYDROXIDE
MAIA Pharmaceuticals, Inc. 1 product
500 mg injectionNDC 70511-0182-84 None of these listed
Show 3 ingredients

ARGININE HYDROCHLORIDE, HYDROCHLORIC ACID, SODIUM HYDROXIDE
Meitheal Pharmaceuticals Inc. 2 products
350 mg/7 mL injectionNDC 71288-0017-15 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
500 mg/10 mL injectionNDC 71288-0016-15 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Mylan Institutional LLC 2 products
500 mg/10 mL injectionNDC 67457-0813-50 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
500 mg/10 mL injectionNDC 67457-0941-15 Sugar (sucrose, dextrose)
Show 2 ingredients

SODIUM HYDROXIDE, SUCROSE
NorthStar RxLLC 2 products
350 mg/7 mL injectionNDC 72603-0147-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
500 mg/10 mL injectionNDC 72603-0152-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
Par Health USA, LLC 1 product
500 mg injectionNDC 42023-0295-10 None of these listed
Show 3 ingredients

ARGININE HYDROCHLORIDE, HYDROCHLORIC ACID, SODIUM HYDROXIDE
Qilu Pharmaceutical Co., Ltd. 1 product
500 mg/10 mL injectionNDC 67184-0549-01 None of these listed
Show 1 ingredient

Sodium Hydroxide
Sagent Pharmaceuticals 2 products
50 mg/mL injectionNDC 25021-0174-15 None of these listed
Show 1 ingredient

sodium hydroxide
350 mg/7 mL injectionNDC 25021-0179-15 None of these listed
Show 1 ingredient

sodium hydroxide
Sintetica US LLC 1 product
500 mg/20 mL injectionNDC 83090-0011-01 No inactive-ingredient list on the label No list we could read
Slate Run Pharmaceuticals, LLC 1 product
500 mg/20 mL injectionNDC 70436-0033-80 No inactive-ingredient list on the label No list we could read
Xellia Pharmaceuticals USA LLC 4 products
350 mg/7 mL injectionNDC 70594-0053-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
350 mg/7 mL injectionNDC 70594-0066-01 None of these listed
Show 4 ingredients

ARGININE, HISTIDINE, HYDROCHLORIC ACID, ISOLEUCINE
500 mg/10 mL injectionNDC 70594-0034-01 None of these listed
Show 1 ingredient

SODIUM HYDROXIDE
500 mg/10 mL injectionNDC 70594-0060-01 None of these listed
Show 4 ingredients

ARGININE, HISTIDINE, HYDROCHLORIC ACID, ISOLEUCINE

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.

Daptomycin without sorbitol or mannitol

Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 1 of 44 checked products list sorbitol or mannitol; 43 do not.

Does not list sorbitol or mannitol

Lists sorbitol or mannitol

Daptomycin without sugar (sucrose or dextrose)

Sugar (sucrose, dextrose): A consideration in diabetes, mostly in liquids and chewables. 1 of 44 checked products list sugar (sucrose or dextrose); 43 do not.

Does not list sugar (sucrose or dextrose)

Lists sugar (sucrose or dextrose)

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 Daptomycin product suits you →

Common questions about Daptomycin inactive ingredients

Is Daptomycin gluten-free?
This page cannot certify any Daptomycin product gluten-free; it reports what each label declares. Of the 44 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 Daptomycin contain lactose?
No checked Daptomycin 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 Daptomycin contain soy?
No checked Daptomycin 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 Daptomycin?
No checked Daptomycin 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 Daptomycin contain gelatin?
No checked Daptomycin 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 Daptomycin 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 Daptomycin guide