Inactive ingredients by manufacturer

Leuprolide inactive ingredients by manufacturer

Wondering whether your Leuprolide 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 Leuprolide 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 8 of the 42 current Leuprolide products on the market today, from 18 companies listing it with the FDA, and lined them up side by side. 10 are still being read and will appear on a later visit. 24 labels have no inactive-ingredient list we could read, so those products cannot be compared.

Ask about your bottle

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

  1. LactoseNo checked product

    No checked Leuprolide product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Leuprolide product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Leuprolide product lists soy.

  4. Synthetic dyesNo checked product

    No checked Leuprolide product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Leuprolide product lists gelatin.

Also listed by some products: Benzyl alcohol 1 of 8

Find a version without it

Every current Leuprolide product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
AbbVie Inc. 12 products
kitsNDC 00074-2282-03 No inactive-ingredient list on the label No list we could read
kitsNDC 00074-2440-03 No inactive-ingredient list on the label No list we could read
kitsNDC 00074-9694-03 Still being read Not read yet
kitsNDC 00074-3779-03 Still being read Not read yet
kitsNDC 00074-3346-03 No inactive-ingredient list on the label No list we could read
kitsNDC 00074-3683-03 No inactive-ingredient list on the label No list we could read
kitsNDC 00074-3473-03 No inactive-ingredient list on the label No list we could read
kitsNDC 00074-3663-03 No inactive-ingredient list on the label No list we could read
kitsNDC 00074-3575-01 No inactive-ingredient list on the label No list we could read
kitsNDC 00074-3642-03 No inactive-ingredient list on the label No list we could read
kitsNDC 00074-2108-03 No inactive-ingredient list on the label No list we could read
kitsNDC 00074-3641-03 No inactive-ingredient list on the label No list we could read
Accord BioPharma, Inc. 2 products
42 mg/0.37 g injectionNDC 69448-0014-63 Still being read Not read yet
42 mg/0.37 g injectionNDC 69448-0023-63 None of these listed
Show 2 ingredients

METHYLPYRROLIDONE, POLYLACTIDE
Amneal Pharmaceuticals LLC 1 product
kitsNDC 70121-2537-06 No inactive-ingredient list on the label No list we could read
Avyxa Pharma, LLC 1 product
kitsNDC 83831-0134-01 No inactive-ingredient list on the label No list we could read
Cipla Usa Inc. 1 product
kitsNDC 69097-0909-50 No inactive-ingredient list on the label No list we could read
Endo USA, Inc. 1 product
1 mg/0.2 mL injectionNDC 42023-0259-00 Benzyl alcohol
Show 5 ingredients

ACETIC ACID, BENZYL ALCOHOL, sodium chloride, SODIUM HYDROXIDE, WATER
Eugia US LLC 1 product
kitsNDC 55150-0478-01 No inactive-ingredient list on the label No list we could read
Meitheal Pharmaceuticals Inc 1 product
kitsNDC 71288-0569-90 No inactive-ingredient list on the label No list we could read
NorthStar RxLLC 1 product
kitsNDC 72603-0344-01 No inactive-ingredient list on the label No list we could read
PAI Holdings, LLC dba PAI Pharma 1 product
kitsNDC 00121-2106-02 No inactive-ingredient list on the label No list we could read
Sandoz Inc 1 product
kitsNDC 00781-4003-32 Still being read Not read yet
Sun Pharmaceutical Industries, Inc. 1 product
kitsNDC 47335-0936-40 Still being read Not read yet
TOLMAR Inc. 10 products
7.5 mg/0.25 mL injectionNDC 62935-0756-80 Still being read Not read yet
22.5 mg/0.375 mL injectionNDC 62935-0227-10 Still being read Not read yet
30 mg/0.5 mL injectionNDC 62935-0306-40 None of these listed
Show 2 ingredients

METHYL PYRROLIDONE, POLY(DL-LACTIC-CO-GLYCOLIC ACID), (75:25; 20000 MW)
45 mg/0.375 mL injectionNDC 62935-0163-60 None of these listed
Show 2 ingredients

METHYL PYRROLIDONE, POLY(DL-LACTIC-CO-GLYCOLIC ACID), (85:15; 23000 MW)
45 mg/0.375 mL injectionNDC 62935-0461-50 None of these listed
Show 2 ingredients

METHYL PYRROLIDONE, POLY(DL-LACTIC-CO-GLYCOLIC ACID), (85:15; 23000 MW)
kitsNDC 62935-0223-05 No inactive-ingredient list on the label No list we could read
kitsNDC 62935-0753-75 No inactive-ingredient list on the label No list we could read
kitsNDC 62935-0153-50 No inactive-ingredient list on the label No list we could read
kitsNDC 62935-0453-45 Still being read Not read yet
kitsNDC 62935-0303-30 Still being read Not read yet
UBI Pharma Inc. 1 product
kitsNDC 72843-0591-99 No inactive-ingredient list on the label No list we could read
Uronova Pharmaceuticals, Inc. 4 products
7.5 mg/0.25 mL injectionNDC 85043-0075-05 None of these listed
Show 2 ingredients

METHYL PYRROLIDONE, POLY(DL-LACTIC-CO-GLYCOLIC ACID), (50:50; 46000 MW)
22.5 mg/0.375 mL injectionNDC 85043-0025-02 Still being read Not read yet
30 mg/0.5 mL injectionNDC 85043-0030-03 None of these listed
Show 2 ingredients

METHYL PYRROLIDONE, POLY(DL-LACTIC-CO-GLYCOLIC ACID), (75:25; 20000 MW)
45 mg/0.375 mL injectionNDC 85043-0045-04 None of these listed
Show 2 ingredients

METHYL PYRROLIDONE, POLY(DL-LACTIC-CO-GLYCOLIC ACID), (85:15; 23000 MW)
VGYAAN Pharmaceuticals LLC 1 product
kitsNDC 72664-0611-28 No inactive-ingredient list on the label No list we could read
Zydus Pharmaceuticals USA Inc. 1 product
kitsNDC 70710-1769-03 No inactive-ingredient list on the label No list we could read
Zydus Lifesciences Limited 1 product
kitsNDC 70771-1687-03 No inactive-ingredient list on the label No list we could read

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.

Leuprolide without benzyl alcohol

Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 1 of 8 checked products list benzyl alcohol; 7 do not.

Does not list benzyl alcohol

Lists benzyl alcohol

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 Leuprolide product suits you →

Common questions about Leuprolide inactive ingredients

Is Leuprolide gluten-free?
This page cannot certify any Leuprolide product gluten-free; it reports what each label declares. Of the 8 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 Leuprolide contain lactose?
No checked Leuprolide 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 Leuprolide contain soy?
No checked Leuprolide 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 Leuprolide?
No checked Leuprolide 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 Leuprolide contain gelatin?
No checked Leuprolide 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, dose form and how it is absorbed; its fillers, binders, coatings and colorants are the manufacturer's own choice. That is why one Leuprolide product can list lactose and a dye while another from a different company lists neither.
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 5, 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 Leuprolide 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 Leuprolide guide