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
7133514251
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-1)
ndc11
7133514252
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-2)
ndc11
7133514253
18 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-3)
ndc11
7133514254
28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-4)
ndc11
7133514255
56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-5)
ndc11
7133514256
58 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-6)
ndc11
7133514257
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-7)
ndc11
7133514258
180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-8)
ndc11
7133514259
120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-9)

Annotations

UNII (FDA Substance ID)

0K5C5T2QPG

LANSOPRAZOLE

RxCUI 17128

Orange Book

A205868

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": "71335-1425_40271c8f-06d7-42c1-a983-8d49f0205268",
  "productndc": "71335-1425",
  "dosage_form": "CAPSULE, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "205868",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "15MG",
        "product_no": "001",
        "approval_date": "Aug 30, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "30MG",
        "product_no": "002",
        "approval_date": "Aug 30, 2017"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LANSOPRAZOLE",
  "proprietary_name": "Lansoprazole",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA205868",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Lansoprazole",
  "start_marketing_date": "20180604",
  "active_numerator_strength": "30"
}

Related drugs

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