Inactive ingredients by manufacturer

Alfuzosin inactive ingredients by manufacturer

Wondering whether your Alfuzosin 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 Alfuzosin 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 17 of the 17 current Alfuzosin products on the market today, from 11 companies listing it with the FDA, and lined them up side by side.

Ask about your bottle

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

  1. LactoseDiffers by manufacturer
  2. Wheat or gluten sourceNo checked product

    No checked Alfuzosin product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Alfuzosin product lists soy.

  4. Synthetic dyesNo checked product

    No checked Alfuzosin product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Alfuzosin product lists gelatin.

Also listed by some products: Corn 4 of 17 Titanium dioxide 5 of 17 Propylene glycol 5 of 17 Sorbitol or mannitol 1 of 17 Sugar 4 of 17

Find a version without it

Every current Alfuzosin product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
Advanz Pharma (US) Corp. 1 product
10 mg extended-release tabletNDC 59212-0200-10 Sorbitol or mannitol
Show 9 ingredients

cellulose, microcrystalline, ethylcellulose (100 mpa.s), ferric oxide yellow, hydrogenated castor oil, hypromelloses, magnesium stearate, mannitol, POVIDONE, UNSPECIFIED, silicon dioxide

Aphena Pharma Solutions - Tennessee, LLC 1 product
10 mg extended-release tabletNDC 43353-0945-16 None of these listed
Show 5 ingredients

CELLULOSE, MICROCRYSTALLINE, GUAR GUM, HYPROMELLOSES, MAGNESIUM STEARATE, SILICON DIOXIDE

Apotex Corp. 1 product
10 mg extended-release tabletNDC 60505-2850-09 None of these listed
Show 5 ingredients

DIBASIC CALCIUM PHOSPHATE DIHYDRATE, FERRIC OXIDE YELLOW, HYPROMELLOSE 2208 (4000 MPA.S), MAGNESIUM STEARATE, POLYVINYL ACETATE PHTHALATE

Aurobindo Pharma Limited 2 products
10 mg extended-release tabletNDC 65862-0249-01 Titanium dioxide Propylene glycol Sugar (sucrose, dextrose)
Show 10 ingredients

ANHYDROUS DIBASIC CALCIUM PHOSPHATE, CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED), HYDROGENATED COTTONSEED OIL, HYPROMELLOSE 2208 (100 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), MAGNESIUM STEARATE, POVIDONE K30, PROPYLENE GLYCOL, SILICON DIOXIDE, TITANIUM DIOXIDE

10 mg extended-release tabletNDC 84386-0153-01 Titanium dioxide Propylene glycol
Show 10 ingredients

ANHYDROUS DIBASIC CALCIUM PHOSPHATE, CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED), HYDROGENATED COTTONSEED OIL, HYPROMELLOSE 2208 (100000 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), MAGNESIUM STEARATE, POVIDONE K30, PROPYLENE GLYCOL, SILICON DIOXIDE, TITANIUM DIOXIDE

Bryant Ranch Prepack 4 products
10 mg extended-release tabletNDC 72162-1449-09 Corn-derived
Show 7 ingredients

DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER, HYDROXYPROPYL CELLULOSE (1600000 WAMW), HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN, TALC

10 mg extended-release tabletNDC 71335-2146-01 Corn-derived
Show 7 ingredients

DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER, HYDROXYPROPYL CELLULOSE (1600000 WAMW), HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN, TALC

10 mg extended-release tabletNDC 63629-9155-01 Lactose
Show 6 ingredients

HYPROMELLOSE 2208 (100000 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE K30, SILICON DIOXIDE

10 mg extended-release tabletNDC 71335-2578-01 Titanium dioxide Propylene glycol Sugar (sucrose, dextrose)
Show 10 ingredients

ANHYDROUS DIBASIC CALCIUM PHOSPHATE, CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED), HYDROGENATED COTTONSEED OIL, HYPROMELLOSE 2208 (100 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), MAGNESIUM STEARATE, POVIDONE K30, PROPYLENE GLYCOL, SILICON DIOXIDE, TITANIUM DIOXIDE

Cipla USA Inc. 1 product
10 mg tabletNDC 69097-0844-02 None of these listed
Show 5 ingredients

GUAR GUM, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE

Exelan Pharmaceuticals Inc. 1 product
10 mg extended-release tabletNDC 76282-0302-01 None of these listed
Show 5 ingredients

CELLULOSE, MICROCRYSTALLINE, GUAR GUM, HYPROMELLOSES, MAGNESIUM STEARATE, SILICON DIOXIDE

Northwind Health Company, LLC 3 products
10 mg extended-release tabletNDC 51655-0432-52 Corn-derived
Show 7 ingredients

DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER, HYDROXYPROPYL CELLULOSE (1600000 WAMW), HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN, TALC

10 mg extended-release tabletNDC 51655-0967-52 Lactose
Show 6 ingredients

HYPROMELLOSE 2208 (100000 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE K30, SILICON DIOXIDE

10 mg extended-release tabletNDC 51655-0087-52 Titanium dioxide Propylene glycol Sugar (sucrose, dextrose)
Show 10 ingredients

ANHYDROUS DIBASIC CALCIUM PHOSPHATE, CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED), HYDROGENATED COTTONSEED OIL, HYPROMELLOSE 2208 (100 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), MAGNESIUM STEARATE, POVIDONE K30, PROPYLENE GLYCOL, SILICON DIOXIDE, TITANIUM DIOXIDE

Rising Pharma Holdings, Inc. 1 product
10 mg extended-release tabletNDC 57237-0114-01 Titanium dioxide Propylene glycol Sugar (sucrose, dextrose)
Show 10 ingredients

ANHYDROUS DIBASIC CALCIUM PHOSPHATE, CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED), HYDROGENATED COTTONSEED OIL, HYPROMELLOSE 2208 (100 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), MAGNESIUM STEARATE, POVIDONE K30, PROPYLENE GLYCOL, SILICON DIOXIDE, TITANIUM DIOXIDE

Sun Pharmaceutical Industries, Inc. 1 product
10 mg extended-release tabletNDC 47335-0956-08 Corn-derived
Show 7 ingredients

DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER, HYDROXYPROPYL CELLULOSE (1600000 WAMW), HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN, TALC

Unichem Pharmaceuticals (USA), Inc. 1 product
10 mg extended-release tabletNDC 29300-0155-01 Lactose
Show 6 ingredients

HYPROMELLOSE 2208 (100000 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE K30, SILICON DIOXIDE

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.

Alfuzosin without lactose

Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 3 of 17 checked products list lactose; 14 do not.

Alfuzosin without corn-derived ingredients

Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. 4 of 17 checked products list corn-derived ingredients; 13 do not.

Alfuzosin without titanium dioxide

Titanium dioxide: A white colorant some people choose to avoid. 5 of 17 checked products list titanium dioxide; 12 do not.

Alfuzosin without propylene glycol

Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 5 of 17 checked products list propylene glycol; 12 do not.

Alfuzosin without sorbitol or mannitol

Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 1 of 17 checked products list sorbitol or mannitol; 16 do not.

Alfuzosin without sugar (sucrose or dextrose)

Sugar (sucrose, dextrose): A consideration in diabetes, mostly in liquids and chewables. 4 of 17 checked products list sugar (sucrose or dextrose); 13 do not.

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 Alfuzosin product suits you →

Common questions about Alfuzosin inactive ingredients

Is Alfuzosin gluten-free?
This page cannot certify any Alfuzosin product gluten-free; it reports what each label declares. Of the 17 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 Alfuzosin contain lactose?
3 of 17 checked Alfuzosin products list lactose; 14 do not: Advanz (10 mg extended-release tablet), Aphena Pharma Solutions - Tennessee (10 mg extended-release tablet), Apotex (10 mg extended-release tablet) and Aurobindo (10 mg extended-release tablet) and 6 other companies. The lactose in a tablet or capsule is a small amount, but people with a milk allergy or a strong intolerance often prefer a version that does not list it.
Does Alfuzosin contain soy?
No checked Alfuzosin 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 Alfuzosin?
No checked Alfuzosin 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 Alfuzosin contain gelatin?
No checked Alfuzosin 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 Alfuzosin 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 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 Alfuzosin 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 Alfuzosin guide