Gluten Screen

Last verified May 17, 2026 · 12 product labels screened

Is lansoprazole gluten-free?

Some formulations contain gluten. Of 12 product labels we cross-checked, 2 list a gluten-derived ingredient outright. Generics from different manufacturers can differ — check which manufacturer's version your pharmacy dispensed before assuming any fill is safe.

Drug context

About lansoprazole

Lansoprazole is a proton-pump inhibitor used for acid reflux and ulcers, sold under brand names including Prevacid.

Why this matters

Different manufacturers, different ingredients

Generics of lansoprazole use the same active ingredient, but they aren't required to use the same inactive ingredients. Your pharmacy may switch which manufacturer they dispense between fills, sometimes without telling you. The list below shows each manufacturer's product label as a separate entry, because that's the granularity that actually matters when you're celiac.

The labels

The 12 we checked

  1. 01
    Rugby Laboratories contains gluten

    Mangione 2024 · lansoprazole 15 mg delayed-release capsule [Rugby Laboratories] · label dated 2025-06-09

    Gluten on the label: Manufacturer-declared gluten content (Matson et al. 2025 (peer-reviewed): the manufacturer of this NDC confirmed that the product contains gluten.)

    View source label →
  2. 02
    Rugby Laboratories contains gluten

    Mangione 2024 · lansoprazole 15 mg delayed-release capsule [Rugby Laboratories] · label dated 2025-06-09

    Gluten on the label: Manufacturer-declared gluten content (Matson et al. 2025 (peer-reviewed): the manufacturer of this NDC confirmed that the product contains gluten.)

    View source label →
  3. 03
    AMERISOURCEBERGEN DRUG CORPORATION nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [AMERISOURCEBERGEN DRUG CORPORATION] · label dated Apr 20, 2026

    Inactive ingredients D&C RED NO. 28 · FD&C BLUE NO. 1 · FD&C GREEN NO. 3 · FD&C RED NO. 40 · FERROSOFERRIC OXIDE · GELATIN · HYDROXYPROPYL CELLULOSE, UNSPECIFIED · LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED · MAGNESIUM CARBONATE · METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER · POLYETHYLENE GLYCOL 6000 · POLYSORBATE 80 · SODIUM LAURYL SULFATE · STARCH, CORN · SUCROSE · TALC · TITANIUM DIOXIDE

    View source label →
  4. 04
    Asclemed USA, Inc. nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [ASCLEMED USA, INC.] · label dated Mar 26, 2026

    Inactive ingredients AMMONIA · D&C RED NO. 28 · FD&C BLUE NO. 1 · FD&C RED NO. 40 · GELATIN, UNSPECIFIED · HYPROMELLOSE 2910 (3 MPA.S) · MAGNESIUM CARBONATE · METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A · POLYETHYLENE GLYCOL 6000 · POLYSORBATE 80 · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · SILICON DIOXIDE · SODIUM LAURYL SULFATE · SUCROSE · TALC · TITANIUM DIOXIDE

    View source label →
  5. 05
    Walgreen Company nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE [WALGREEN COMPANY] · label dated Mar 02, 2026

    Inactive ingredients ASCORBIC ACID · CETYL ALCOHOL · COPOVIDONE K25-31 · CROSPOVIDONE, UNSPECIFIED · HYPROMELLOSE, UNSPECIFIED · MALTITOL · MANNITOL · MEGLUMINE · MICROCRYSTALLINE CELLULOSE · POLYSORBATE 80 · PROPYLENE GLYCOL · SILICON DIOXIDE · SODIUM STEARYL FUMARATE · SORBITOL · SUCRALOSE · TALC · TITANIUM DIOXIDE · TRIETHYL CITRATE

    View source label →
  6. 06
    Medcore LLC nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [MEDCORE LLC] · label dated Jan 21, 2026

    Inactive ingredients AMMONIA · D&C RED NO. 28 · FD&C BLUE NO. 1 · FD&C RED NO. 40 · GELATIN, UNSPECIFIED · HYPROMELLOSE 2910 (3 MPA.S) · MAGNESIUM CARBONATE · METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER · POLYETHYLENE GLYCOL 6000 · POLYSORBATE 80 · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · SILICON DIOXIDE · SODIUM LAURYL SULFATE · SUCROSE · TALC · TITANIUM DIOXIDE

    View source label →
  7. 07
    Ajanta Pharma USA Inc. nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [AJANTA PHARMA USA INC.] · label dated Dec 08, 2025

    Inactive ingredients AMMONIA · FERRIC OXIDE RED · FERRIC OXIDE YELLOW · FERROSOFERRIC OXIDE · HYDROXYPROPYL CELLULOSE (1600000 WAMW) · HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED · HYPROMELLOSE, UNSPECIFIED · MAGNESIUM CARBONATE · METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A · POLYETHYLENE GLYCOL, UNSPECIFIED · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · SILICON DIOXIDE · SODIUM BICARBONATE · SODIUM LAURYL SULFATE · SUCROSE · TALC

    View source label →
  8. 08
    Amerisource Bergen nothing flagged on the label

    US label (DailyMed) · GOOD NEIGHBOR PHARMACY LANSOPRAZOLE (LANSOPRAZOLE) CAPSULE, DELAYED RELEASE [AMERISOURC… · label dated Dec 04, 2025

    Inactive ingredients D&C RED NO. 28 · D&C YELLOW NO. 10 · FD&C BLUE NO. 1 · FD&C RED NO. 40 · GELATIN, UNSPECIFIED · HYPROMELLOSE, UNSPECIFIED · LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED · MANNITOL · MEGLUMINE · METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYSORBATE 80 · SODIUM LAURYL SULFATE · TALC · TITANIUM DIOXIDE

    View source label →
  9. 09
    Mylan Institutional Inc. nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE PELLETS [MYLAN INSTITUTIONAL INC.] · label dated Nov 17, 2025

    Inactive ingredients AMMONIA · FD&C BLUE NO. 1 · FD&C RED NO. 3 · FERROSOFERRIC OXIDE · GELATIN, UNSPECIFIED · HYDROXYPROPYL CELLULOSE (1600000 WAMW) · LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED · MAGNESIUM CARBONATE · METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYSORBATE 80 · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · SILICON DIOXIDE · STARCH, CORN · SUCROSE · TALC · TITANIUM DIOXIDE

    View source label →
  10. 10
    Rite Aid Corporation nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [RITE AID CORPORATION] · label dated Aug 27, 2025

    Inactive ingredients AMMONIA · FD&C BLUE NO. 1 · FD&C RED NO. 3 · FD&C RED NO. 40 · FERRIC OXIDE YELLOW · FERROSOFERRIC OXIDE · GELATIN · HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED · HYDROXYPROPYL CELLULOSE, UNSPECIFIED · MAGNESIUM CARBONATE · METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYSORBATE 80 · SHELLAC · SILICON DIOXIDE · STARCH, CORN · SUCROSE · TALC · TITANIUM DIOXIDE

    View source label →
  11. 11
    CVS Pharmacy nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [CVS PHARMACY] · label dated Aug 22, 2025

    Inactive ingredients AMMONIA · FD&C BLUE NO. 1 · FD&C RED NO. 3 · FD&C RED NO. 40 · FERRIC OXIDE YELLOW · FERROSOFERRIC OXIDE · GELATIN · HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED · HYDROXYPROPYL CELLULOSE, UNSPECIFIED · MAGNESIUM CARBONATE · METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYSORBATE 80 · SHELLAC · SILICON DIOXIDE · STARCH, CORN · SUCROSE · TALC · TITANIUM DIOXIDE

    View source label →
  12. 12
    Ascend Laboratories, LLC nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [ASCEND LABORATORIES, LLC] · label dated Jul 23, 2025

    Inactive ingredients AMMONIA · D&C RED NO. 28 · FD&C BLUE NO. 1 · FD&C GREEN NO. 3 · FD&C RED NO. 40 · GELATIN, UNSPECIFIED · HYPROMELLOSE 2910 (3 MPA.S) · MAGNESIUM CARBONATE · METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A · POLYETHYLENE GLYCOL 6000 · POLYSORBATE 80 · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · SILICON DIOXIDE · SODIUM LAURYL SULFATE · SUCROSE · TALC · TITANIUM DIOXIDE

    View source label →

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Background

What “gluten in a medication” actually means

Gluten enters drugs through their excipients — the inactive ingredients used to bind, coat, fill, or stabilize the dose. The main concern is wheat starch as a filler. Source-ambiguous starches (plain “starch”, pregelatinized starch, sodium starch glycolate, modified starch) get flagged for verification because their botanical origin isn't always disclosed on the label.

The 2024 Mangione et al. pediatric NDC analysis (689 NDCs across the top 100 pediatric medications) found 1.5% contained gluten outright; another 25.7% couldn't be confirmed either way. Liquid and oral-suspension formulations carry disproportionate risk because wheat starch is a common thickener. Full methodology →

Keep checking

Other drugs people look up

Important. This page is informational. Drug labels can change without notice; a manufacturer attestation is point-in-time, not a warranty. If you have celiac disease and your pharmacy switches manufacturers, re-screen the new label before taking the dispensed product. For a definitive answer, call the manufacturer's medical-information line with the NDC code from your prescription bottle.