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United States · US · US:55111-399_c8eb1d41-1fd2-7c06-486c-e6abf08faa6d

Lansoprazole

Orange BookUNIISPLATC A02BC03

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerDr.Reddy's Laboratories Ltd.
CountryUS (United States)
ATC codeA02BC03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    5511139901
    100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-399-01)
  • ndc11
    5511139905
    500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-399-05)
  • ndc11
    5511139930
    30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-399-30)
  • ndc11
    5511139960
    60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-399-60)
  • ndc11
    5511139979
    1 BLISTER PACK in 1 CARTON (55111-399-79) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
  • ndc11
    5511139990
    90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-399-90)

Annotations

UNII (FDA Substance ID)
0K5C5T2QPG
LANSOPRAZOLE
RxCUI 17128
Orange Book
A091269
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": "55111-399_c8eb1d41-1fd2-7c06-486c-e6abf08faa6d",
  "productndc": "55111-399",
  "dosage_form": "CAPSULE, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "091269",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "15MG",
        "product_no": "001",
        "approval_date": "Oct 15, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "30MG",
        "product_no": "002",
        "approval_date": "Oct 15, 2010"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LANSOPRAZOLE",
  "proprietary_name": "Lansoprazole",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA091269",
  "marketing_category": "ANDA",
  "nonproprietary_name": "lansoprazole",
  "start_marketing_date": "20101015",
  "active_numerator_strength": "30"
}

Related drugs

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