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United States · US · US:66993-423_bac21d2f-425d-46ab-ae15-e8cfb373615e

Lanthanum carbonate

Orange BookUNIISPLATC V03AE03

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

Identification

ManufacturerPrasco Laboratories
CountryUS (United States)
ATC codeV03AE03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6699342385
    6 BOTTLE in 1 PACKAGE (66993-423-85) / 15 TABLET, CHEWABLE in 1 BOTTLE (66993-423-53)

Annotations

UNII (FDA Substance ID)
490D9F069T
LANTHANUM CARBONATE
RxCUI 234416
Orange Book
N021468
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "490D9F069T",
    "rxcui": "234416",
    "inchikey": "PKOQIYFBOVTYOH-UHFFFAOYSA-H",
    "display_name": "LANTHANUM CARBONATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "ff444983-e1a4-4c81-b31a-f9e29bde2624": {
      "match": "brand_token",
      "title": "LANTHANUM CARBONATE POWDER [AX PHARMACEUTICAL CORP]",
      "spl_version": "4",
      "published_date": "2026-05-04"
    }
  },
  "productid": "66993-423_bac21d2f-425d-46ab-ae15-e8cfb373615e",
  "productndc": "66993-423",
  "dosage_form": "TABLET, CHEWABLE",
  "orange_book": {
    "appl_no": "021468",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 250MG BASE",
        "product_no": "001",
        "approval_date": "Oct 26, 2004"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 500MG BASE",
        "product_no": "002",
        "approval_date": "Oct 26, 2004"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 750MG BASE",
        "product_no": "003",
        "approval_date": "Nov 23, 2005"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 1GM BASE",
        "product_no": "004",
        "approval_date": "Nov 23, 2005"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LANTHANUM CARBONATE",
  "proprietary_name": "Lanthanum carbonate",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA021468",
  "marketing_category": "NDA AUTHORIZED GENERIC",
  "nonproprietary_name": "LANTHANUM CARBONATE",
  "start_marketing_date": "20170830",
  "active_numerator_strength": "750"
}

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