Gluten Screen

DailyMed checked live · reference data updated August 19, 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
    Amazon.com Services LLC nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [AMAZON.COM SERVICES LLC] · label dated Aug 10, 2026

    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 →
  4. 04
    Walgreens company nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [WALGREENS COMPANY] · label dated Jul 31, 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 →
  5. 05
    Dr. Reddy's Laboratories Limited nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [DR. REDDY'S LABORATORIES LIMITED] · label dated Jul 27, 2026

    Inactive ingredients FD&C BLUE NO. 2 · FERRIC OXIDE RED · FERRIC OXIDE YELLOW · FERROSOFERRIC OXIDE · GELATIN · HYDROXYPROPYL CELLULOSE (110000 WAMW) · Hydroxypropyl Cellulose, Low Substituted · MAGNESIUM CARBONATE · METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A · POLYETHYLENE GLYCOL 6000 · POLYSORBATE 80 · SODIUM LAURYL SULFATE · STARCH, CORN · SUCROSE · TALC · TITANIUM DIOXIDE

    View source label →
  6. 06
    Dr. Reddy's Laboratories Inc. nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [DR. REDDY'S LABORATORIES INC.] · label dated Jul 27, 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 →
  7. 07
    Chain Drug Marketing Association nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [CHAIN DRUG MARKETING ASSOCIATION] · label dated Jul 24, 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 →
  8. 08
    Redpharm Drug nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [REDPHARM DRUG] · label dated Jul 20, 2026

    Inactive ingredients AMMONIA · FERRIC OXIDE RED · FERRIC OXIDE YELLOW · FERROSOFERRIC OXIDE · GELATIN, UNSPECIFIED · HYDROXYPROPYL CELLULOSE (1600000 WAMW) · LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED · MAGNESIUM CARBONATE · METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYSORBATE 80 · PROPYLENE GLYCOL · RAW SUGAR · SHELLAC · SODIUM LAURYL SULFATE · STARCH, CORN · SUCROSE · TALC · TITANIUM DIOXIDE

    View source label →
  9. 09
    Rugby Laboratories, Inc nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [RUGBY LABORATORIES, INC] · label dated Jul 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 →
  10. 10
    NorthStar Rx LLC nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE [NORTHSTAR RX LLC] · label dated Jul 17, 2026

    Inactive ingredients Anhydrous Citric Acid · Aspartame · Cellulose, Microcrystalline · Crospovidone · Ethyl Acrylate and Methyl Methacrylate Copolymer Dispersion (2:1; 750000 MW 30% AQUEOUS) · Ferric Oxide Red · Ferric Oxide Yellow · Glyceryl Monostearate · Hydroxypropyl Cellulose (90000 Wamw) · Hypromellose 2910 (15 Mpa.S) · Hypromellose 2910 (3 Mpa.S) · Low-Substituted Hydroxypropyl Cellulose, Unspecified · Magnesium Carbonate · Magnesium Stearate · Mannitol · Methacrylic Acid and Ethyl Acrylate Copolymer · Polyethylene Glycol 6000 · Polysorbate 80 · Sodium Hydroxide · Strawberry · Sucrose · Triethyl Citrate · talc · titanium dioxide

    View source label →
  11. 11
    Dr. Reddy's Laboratories Inc. nothing flagged on the label

    US label (DailyMed) · LANSOPRAZOLE CAPSULE, DELAYED RELEASE [DR. REDDY'S LABORATORIES INC.] · label dated Jul 17, 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 →
  12. 12
    Retail Business Services, LLC nothing flagged on the label

    US label (DailyMed) · CAREONE ACID REDUCER (LANSOPRAZOLE) CAPSULE, DELAYED RELEASE [RETAIL BUSINESS SERVICES,… · label dated Jul 10, 2026

    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 →

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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

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More from Gluten Screen

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 — or take our printable pharmacist card to the counter, which asks the three questions a pharmacist can actually answer.