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United States · US · US:76420-907_2cbe759e-e896-7ada-e063-6394a90a6cc5

Lubiprostone

Orange BookUNIISPLATC A06AX03

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

Identification

ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC codeA06AX03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    7642090701
    100 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-907-01)
  • ndc11
    7642090730
    30 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-907-30)
  • ndc11
    7642090760
    60 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-907-60)
  • ndc11
    7642090790
    90 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-907-90)

Annotations

UNII (FDA Substance ID)
7662KG2R6K
LUBIPROSTONE
RxCUI 623033
Orange Book
N021908
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "7662KG2R6K",
    "rxcui": "623033",
    "inchikey": "WGFOBBZOWHGYQH-MXHNKVEKSA-N",
    "display_name": "LUBIPROSTONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "f4d506e0-1322-4fc4-e053-2995a90ac880": {
      "match": "brand_token",
      "title": "LUBIPROSTONE CAPSULE, GELATIN COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]",
      "spl_version": "5",
      "published_date": "2026-05-11"
    }
  },
  "productid": "76420-907_2cbe759e-e896-7ada-e063-6394a90a6cc5",
  "productndc": "76420-907",
  "dosage_form": "CAPSULE, GELATIN COATED",
  "orange_book": {
    "appl_no": "021908",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "24MCG",
        "product_no": "001",
        "approval_date": "Jan 31, 2006"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "8MCG",
        "product_no": "002",
        "approval_date": "Apr 29, 2008"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LUBIPROSTONE",
  "proprietary_name": "Lubiprostone",
  "active_ingred_unit": "ug/1",
  "application_number": "NDA021908",
  "marketing_category": "NDA AUTHORIZED GENERIC",
  "nonproprietary_name": "lubiprostone",
  "start_marketing_date": "20230101",
  "active_numerator_strength": "24"
}

Related drugs

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