Inactive ingredients by manufacturer

Hydrochlorothiazide / Telmisartan inactive ingredients by manufacturer

Wondering whether your Hydrochlorothiazide / Telmisartan 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 Hydrochlorothiazide / Telmisartan 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 24 of the 27 current Hydrochlorothiazide / Telmisartan products on the market today, from 9 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 Hydrochlorothiazide / Telmisartan? 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 Hydrochlorothiazide / Telmisartan products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseEvery checked product

    Every checked Hydrochlorothiazide / Telmisartan product (24) lists lactose. See the products

  2. Wheat or gluten sourceNo checked product

    No checked Hydrochlorothiazide / Telmisartan product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Hydrochlorothiazide / Telmisartan product lists soy.

  4. Synthetic dyesNo checked product

    No checked Hydrochlorothiazide / Telmisartan product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Hydrochlorothiazide / Telmisartan product lists gelatin.

Also listed by some products: Sorbitol or mannitol 21 of 24

Find a version without it

Every current Hydrochlorothiazide / Telmisartan product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
Alembic Pharmaceuticals Inc. 3 products
TELMISARTAN 40 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 62332-0209-10 Lactose Sorbitol or mannitol
Show 8 ingredients

FERRIC OXIDE RED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE K25, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 62332-0210-10 Lactose Sorbitol or mannitol
Show 8 ingredients

FERRIC OXIDE RED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE K25, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 25 mg tabletNDC 62332-0211-10 Lactose Sorbitol or mannitol
Show 8 ingredients

FERRIC OXIDE YELLOW, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE K25, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
Alembic Pharmaceuticals Limited 3 products
TELMISARTAN 40 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 46708-0209-10 Lactose Sorbitol or mannitol
Show 8 ingredients

FERRIC OXIDE RED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE K25, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 46708-0210-10 Lactose Sorbitol or mannitol
Show 8 ingredients

FERRIC OXIDE RED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE K25, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 25 mg tabletNDC 46708-0211-10 Lactose Sorbitol or mannitol
Show 8 ingredients

FERRIC OXIDE YELLOW, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE K25, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
Aurobindo Pharma Limited 3 products
TELMISARTAN 40 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 65862-0976-03 Lactose Sorbitol or mannitol
Show 9 ingredients

FERRIC OXIDE RED, HYDROXYPROPYL CELLULOSE (110000 WAMW), LACTOSE MONOHYDRATE, MANNITOL, MEGLUMINE, POVIDONE K25, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 65862-0977-03 Lactose Sorbitol or mannitol
Show 9 ingredients

FERRIC OXIDE RED, HYDROXYPROPYL CELLULOSE (110000 WAMW), LACTOSE MONOHYDRATE, MANNITOL, MEGLUMINE, POVIDONE K25, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 25 mg tabletNDC 65862-0978-03 Lactose Sorbitol or mannitol
Show 9 ingredients

FERRIC OXIDE YELLOW, HYDROXYPROPYL CELLULOSE (110000 WAMW), LACTOSE MONOHYDRATE, MANNITOL, MEGLUMINE, POVIDONE K25, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
AvKARE 3 products
TELMISARTAN 40 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 42291-0462-30 Lactose Sorbitol or mannitol
Show 12 ingredients

CROSPOVIDONE (120 .MU.M), FERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE, UNSPECIFIED, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE, TALC
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 42291-0463-30 Lactose Sorbitol or mannitol
Show 12 ingredients

CROSPOVIDONE (120 .MU.M), FERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE, UNSPECIFIED, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE, TALC
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 25 mg tabletNDC 42291-0464-30 Lactose Sorbitol or mannitol
Show 13 ingredients

CROSPOVIDONE (120 .MU.M), FERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE, UNSPECIFIED, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE, TALC
Boehringer Ingelheim Pharmaceuticals, Inc. 3 products
TELMISARTAN 40 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 00597-0043-37 No inactive-ingredient list on the label No list we could read
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 00597-0044-37 No inactive-ingredient list on the label No list we could read
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 25 mg tabletNDC 00597-0042-37 No inactive-ingredient list on the label No list we could read
Glenmark Pharmaceuticals Inc., USA 3 products
TELMISARTAN 40 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 68462-0840-13 Lactose Sorbitol or mannitol
Show 12 ingredients

CROSPOVIDONE (120 .MU.M), FERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE, UNSPECIFIED, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE, TALC
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 68462-0841-13 Lactose Sorbitol or mannitol
Show 12 ingredients

CROSPOVIDONE (120 .MU.M), FERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE, UNSPECIFIED, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE, TALC
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 25 mg tabletNDC 68462-0842-13 Lactose Sorbitol or mannitol
Show 13 ingredients

CROSPOVIDONE (120 .MU.M), FERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, POVIDONE, UNSPECIFIED, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE, TALC
Lifestar Pharma LLC 3 products
TELMISARTAN 40 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 70756-0315-30 Lactose Sorbitol or mannitol
Show 9 ingredients

FERRIC OXIDE YELLOW, HYDROXYPROPYL CELLULOSE (110000 WAMW), LACTOSE MONOHYDRATE, MANNITOL, MEGLUMINE, POVIDONE K30, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 70756-0316-30 Lactose Sorbitol or mannitol
Show 9 ingredients

FERRIC OXIDE RED, HYDROXYPROPYL CELLULOSE (110000 WAMW), LACTOSE MONOHYDRATE, MANNITOL, MEGLUMINE, POVIDONE K30, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 25 mg tabletNDC 70756-0317-30 Lactose Sorbitol or mannitol
Show 9 ingredients

FERRIC OXIDE YELLOW, HYDROXYPROPYL CELLULOSE (110000 WAMW), LACTOSE MONOHYDRATE, MANNITOL, MEGLUMINE, POVIDONE K30, SILICON DIOXIDE, SODIUM HYDROXIDE, SODIUM STEARYL FUMARATE
Lupin Pharmaceuticals, Inc. 3 products
HYDROCHLOROTHIAZIDE 12.5 mg/1; TELMISARTAN 40 mg tabletNDC 68180-0193-06 Lactose
Show 6 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE, SODIUM HYDROXIDE
HYDROCHLOROTHIAZIDE 12.5 mg/1; TELMISARTAN 80 mg tabletNDC 68180-0194-06 Lactose
Show 6 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE RED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE, SODIUM HYDROXIDE
HYDROCHLOROTHIAZIDE 25 mg/1; TELMISARTAN 80 mg tabletNDC 68180-0195-06 Lactose
Show 6 ingredients

CROSCARMELLOSE SODIUM, FERRIC OXIDE YELLOW, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POVIDONE, SODIUM HYDROXIDE
Solco Healthcare LLC 3 products
TELMISARTAN 40 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 43547-0441-03 Lactose Sorbitol or mannitol
Show 12 ingredients

CROSPOVIDONE (120 .MU.M), FERRIC OXIDE RED, HYPROMELLOSE 2910 (5 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED, SODIUM HYDROXIDE, SODIUM STARCH GLYCOLATE TYPE A POTATO, SODIUM STEARYL FUMARATE
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 12.5 mg tabletNDC 43547-0442-03 Lactose Sorbitol or mannitol
Show 12 ingredients

CROSPOVIDONE (120 .MU.M), FERRIC OXIDE RED, HYPROMELLOSE 2910 (5 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED, SODIUM HYDROXIDE, SODIUM STARCH GLYCOLATE TYPE A POTATO, SODIUM STEARYL FUMARATE
TELMISARTAN 80 mg/1; HYDROCHLOROTHIAZIDE 25 mg tabletNDC 43547-0443-03 Lactose Sorbitol or mannitol
Show 12 ingredients

CROSPOVIDONE (120 .MU.M), FERRIC OXIDE YELLOW, HYPROMELLOSE 2910 (5 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, MEGLUMINE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED, SODIUM HYDROXIDE, SODIUM STARCH GLYCOLATE TYPE A POTATO, SODIUM STEARYL FUMARATE

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.

Hydrochlorothiazide / Telmisartan and lactose

Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. Every checked Hydrochlorothiazide / Telmisartan product (24) lists lactose.

Lists lactose

Hydrochlorothiazide / Telmisartan without sorbitol or mannitol

Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 21 of 24 checked products list sorbitol or mannitol; 3 do not.

Does not list sorbitol or mannitol

Lists sorbitol or mannitol

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 Hydrochlorothiazide / Telmisartan product suits you →

Common questions about Hydrochlorothiazide / Telmisartan inactive ingredients

Is Hydrochlorothiazide / Telmisartan gluten-free?
This page cannot certify any Hydrochlorothiazide / Telmisartan product gluten-free; it reports what each label declares. Of the 24 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 Hydrochlorothiazide / Telmisartan contain lactose?
Every checked Hydrochlorothiazide / Telmisartan product (24) lists lactose on its label. 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 Hydrochlorothiazide / Telmisartan contain soy?
No checked Hydrochlorothiazide / Telmisartan 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 Hydrochlorothiazide / Telmisartan?
No checked Hydrochlorothiazide / Telmisartan 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 Hydrochlorothiazide / Telmisartan contain gelatin?
No checked Hydrochlorothiazide / Telmisartan 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 Hydrochlorothiazide / Telmisartan 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 Hydrochlorothiazide / Telmisartan 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 Hydrochlorothiazide / Telmisartan guide