Calcitonin Salmon Injection inactive ingredients by manufacturer
Wondering whether your Calcitonin Salmon 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 Calcitonin Salmon 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 11 of the 12 current Calcitonin Salmon Injection products on the market today, from 10 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 Calcitonin Salmon 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 Calcitonin Salmon Injection products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Calcitonin Salmon Injection product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Calcitonin Salmon Injection product lists a wheat or gluten source.
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SoyNo checked product
No checked Calcitonin Salmon Injection product lists soy.
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Synthetic dyesNo checked product
No checked Calcitonin Salmon Injection product lists synthetic dyes.
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GelatinNo checked product
No checked Calcitonin Salmon Injection product lists gelatin.
Find a version without it
Every current Calcitonin Salmon Injection product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Amneal Pharmaceuticals LLC 1 product | ||
| 200 [USP'U]/mL injectionNDC 70121-1650-02 | None of these listed |
Show 5 ingredientsACETIC ACID, PHENOL, SODIUM ACETATE, SODIUM CHLORIDE, WATER |
| Cipla USA Inc. 1 product | ||
| 200 [USP'U]/mL injectionNDC 69097-0770-32 | None of these listed |
Show 5 ingredientsACETIC ACID, PHENOL, SODIUM ACETATE, SODIUM CHLORIDE, WATER |
| Dr. Reddy's Laboratories, Inc. 1 product | ||
| 200 [USP'U]/mL injectionNDC 43598-0051-11 | None of these listed |
Show 5 ingredientsAcetic Acid, Phenol, Sodium Acetate, Sodium Chloride, Water |
| Fresenius Kabi USA, LLC 1 product | ||
| 200 [IU]/mL injectionNDC 63323-0865-02 | None of these listed |
Show 5 ingredientsAcetic acid, Phenol, Sodium Acetate, Sodium chloride, water |
| Hikma Pharmaceuticals USA Inc. 1 product | ||
| 200 [USP'U]/mL injectionNDC 24201-0400-02 | None of these listed |
Show 5 ingredientsACETIC ACID, PHENOL, SODIUM ACETATE, SODIUM CHLORIDE, WATER |
| Mylan Institutional LLC 3 products | ||
| 200 [USP'U]/mL injectionNDC 72078-0039-02 | Still being read | Not read yet |
| 200 [USP'U]/mL injectionNDC 72078-0038-02 | None of these listed |
Show 5 ingredientsACETIC ACID, PHENOL, SODIUM ACETATE, SODIUM CHLORIDE, WATER |
| 200 [USP'U]/mL injectionNDC 67457-0675-02 | None of these listed |
Show 5 ingredientsACETIC ACID, PHENOL, SODIUM ACETATE, SODIUM CHLORIDE, WATER |
| Par Health USA, LLC 1 product | ||
| 200 [IU]/mL injectionNDC 42023-0205-01 | None of these listed |
Show 5 ingredientsACETIC ACID, PHENOL, SODIUM ACETATE, SODIUM CHLORIDE, WATER |
| Sagent Pharmaceuticals 1 product | ||
| 400 [USP'U]/2 mL injectionNDC 25021-0473-02 | None of these listed |
Show 5 ingredientsAcetic Acid, Phenol, Sodium Acetate, Sodium Chloride, Water |
| Zydus Pharmaceuticals USA Inc. 1 product | ||
| 200 [USP'U]/mL injectionNDC 70710-1875-01 | None of these listed |
Show 5 ingredientsACETIC ACID, PHENOL, SODIUM ACETATE, SODIUM CHLORIDE, WATER |
| Zydus Lifesciences Limited 1 product | ||
| 200 [USP'U]/mL injectionNDC 70771-1971-01 | None of these listed |
Show 5 ingredientsACETIC ACID, PHENOL, SODIUM ACETATE, SODIUM CHLORIDE, 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.
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 Calcitonin Salmon Injection inactive ingredients
Is Calcitonin Salmon Injection gluten-free?
Does Calcitonin Salmon Injection contain lactose?
Does Calcitonin Salmon Injection contain soy?
Is there a dye-free Calcitonin Salmon Injection?
Does Calcitonin Salmon Injection 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 Calcitonin Salmon 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 Calcitonin Salmon Injection guide