Lansoprazole

Orange BookUNIISPLATC A02BC03

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeA02BC03

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 9

ndc11
7133518201
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-1)
ndc11
7133518202
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-2)
ndc11
7133518203
18 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-3)
ndc11
7133518204
28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-4)
ndc11
7133518205
56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-5)
ndc11
7133518206
58 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-6)
ndc11
7133518207
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-7)
ndc11
7133518208
180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-8)
ndc11
7133518209
120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-9)

Annotations

UNII (FDA Substance ID)

0K5C5T2QPG

LANSOPRAZOLE

RxCUI 17128

Orange Book

A203203

ABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "0K5C5T2QPG",
    "rxcui": "17128",
    "inchikey": "MJIHNNLFOKEZEW-UHFFFAOYSA-N",
    "display_name": "LANSOPRAZOLE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "c9a43df0-efab-4486-860f-92afdb258c8b": {
      "match": "brand_token",
      "title": "LANSOPRAZOLE TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE [CARDINAL HEALTH 107, LLC]",
      "spl_version": "5",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-1820_e66cf5f3-d909-40ad-a03d-c0423f41aa23",
  "productndc": "71335-1820",
  "dosage_form": "CAPSULE, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "203203",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "15MG",
        "product_no": "001",
        "approval_date": "Jul 25, 2016"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "30MG",
        "product_no": "002",
        "approval_date": "Jul 25, 2016"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LANSOPRAZOLE",
  "proprietary_name": "Lansoprazole",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA203203",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Lansoprazole",
  "start_marketing_date": "20180824",
  "active_numerator_strength": "30"
}

Related drugs

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