Micafungin inactive ingredients by manufacturer
Wondering whether your Micafungin 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 Micafungin 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 22 of the 24 current Micafungin products on the market today, from 12 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 Micafungin? 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 Micafungin products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseDiffers by manufacturer
19 of 22 checked products list lactose; 3 do not. See the products
Does not list it Baxter Healthcare -
Wheat or gluten sourceNo checked product
No checked Micafungin product lists a wheat or gluten source.
-
SoyNo checked product
No checked Micafungin product lists soy.
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Synthetic dyesNo checked product
No checked Micafungin product lists synthetic dyes.
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GelatinNo checked product
No checked Micafungin product lists gelatin.
Find a version without it
Every current Micafungin product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Astellas Pharma US, Inc. 1 product | ||
| 10 mg/mL injectionNDC 00469-3250-10 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| Baxter Healthcare Corporation 3 products | ||
| 50 mg/50 mL injectionNDC 00338-9051-12 | None of these listed |
Show 4 ingredientsANHYDROUS CITRIC ACID, SODIUM CHLORIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| 100 mg/100 mL injectionNDC 00338-9053-12 | None of these listed |
Show 4 ingredientsANHYDROUS CITRIC ACID, SODIUM CHLORIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| 150 mg/150 mL injectionNDC 00338-9055-10 | None of these listed |
Show 4 ingredientsANHYDROUS CITRIC ACID, SODIUM CHLORIDE, TRISODIUM CITRATE DIHYDRATE, WATER |
| Biocon Pharma Inc. 2 products | ||
| 10 mg/mL injectionNDC 70377-0075-91 | Still being read | Not read yet |
| 20 mg/mL injectionNDC 70377-0076-91 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| Fresenius Kabi USA, LLC 2 products | ||
| 50 mg injectionNDC 63323-0728-10 | Lactose |
Show 3 ingredientsAnhydrous Citric Acid, Lactose Monohydrate, Sodium Hydroxide |
| 100 mg injectionNDC 63323-0729-10 | Lactose |
Show 3 ingredientsAnhydrous Citric Acid, Lactose Monohydrate, Sodium Hydroxide |
| Glenmark Pharmaceuticals Inc., USA 2 products | ||
| 10 mg/mL injectionNDC 68462-0771-01 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| 20 mg/mL injectionNDC 68462-0772-01 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| Hikma Pharmaceuticals USA Inc. 2 products | ||
| 50 mg injectionNDC 00143-9361-01 | Lactose |
Show 3 ingredientsCITRIC ACID MONOHYDRATE, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| 100 mg injectionNDC 00143-9362-01 | Lactose |
Show 3 ingredientsCITRIC ACID MONOHYDRATE, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| Hisun Pharmaceuticals USA, Inc. 2 products | ||
| 50 mg injectionNDC 42658-0022-01 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| 100 mg injectionNDC 42658-0023-01 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| Meitheal Pharmaceuticals Inc. 2 products | ||
| 50 mg/5 mL injectionNDC 71288-0028-11 | Still being read | Not read yet |
| 100 mg/5 mL injectionNDC 71288-0029-11 | Lactose |
Show 3 ingredientsanhydrous citric acid, lactose monohydrate, sodium hydroxide |
| Qilu Pharmaceutical Co., Ltd 2 products | ||
| 10 mg/mL injectionNDC 67184-0589-01 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| 20 mg/mL injectionNDC 67184-0590-01 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| Sagent Pharmaceuticals 2 products | ||
| 50 mg/5 mL injectionNDC 25021-0190-10 | Lactose |
Show 4 ingredientsanhydrous citric acid, lactose monohydrate, sodium hydroxide, water |
| 100 mg/5 mL injectionNDC 25021-0191-10 | Lactose |
Show 4 ingredientsanhydrous citric acid, lactose monohydrate, sodium hydroxide, water |
| Zydus Pharmaceuticals USA Inc. 2 products | ||
| 10 mg/mL injectionNDC 70710-1724-01 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| 20 mg/mL injectionNDC 70710-1725-01 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| Zydus Lifesciences Limited 2 products | ||
| 10 mg/mL injectionNDC 70771-1683-01 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
| 20 mg/mL injectionNDC 70771-1684-01 | Lactose |
Show 3 ingredientsANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, SODIUM HYDROXIDE |
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.
Micafungin without lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 19 of 22 checked products list lactose; 3 do not.
Does not list lactose
- Baxter Healthcare: 50 mg/50 mL injection, 100 mg/100 mL injection, 150 mg/150 mL injection
Lists lactose
- Astellas: 10 mg/mL injection
- Biocon: 20 mg/mL injection
- Fresenius Kabi: 50 mg injection, 100 mg injection
- Glenmark: 10 mg/mL injection, 20 mg/mL injection
- Hikma: 50 mg injection, 100 mg injection
- Hisun: 50 mg injection, 100 mg injection
- Meitheal: 100 mg/5 mL injection
- Qilu: 10 mg/mL injection, 20 mg/mL injection
- Sagent: 50 mg/5 mL injection, 100 mg/5 mL injection
- Zydus: 10 mg/mL injection, 20 mg/mL injection
- Zydus Lifesciences: 10 mg/mL injection, 20 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.
Common questions about Micafungin inactive ingredients
Is Micafungin gluten-free?
Does Micafungin contain lactose?
Does Micafungin contain soy?
Is there a dye-free Micafungin?
Does Micafungin 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 Micafungin 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 Micafungin guide