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United States · US · US:72476-109_43e180c4-f363-167e-e063-6394a90ad626

Ibuprofen

Orange BookUNIISPLATC G02CC01

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

Identification

ManufacturerRETAIL BUSINESS SERVICES , LLC.
CountryUS (United States)
ATC codeG02CC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    7247610901
    1 BOTTLE, PLASTIC in 1 CARTON (72476-109-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
  • ndc11
    7247610902
    1 BOTTLE, PLASTIC in 1 CARTON (72476-109-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
  • ndc11
    7247610903
    1 BOTTLE, PLASTIC in 1 CARTON (72476-109-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • ndc11
    7247610905
    500 TABLET, COATED in 1 BOTTLE, PLASTIC (72476-109-05)
  • ndc11
    7247610906
    1000 TABLET, COATED in 1 BOTTLE, PLASTIC (72476-109-06)
  • ndc11
    7247610908
    250 TABLET, COATED in 1 BOTTLE, PLASTIC (72476-109-08)
  • ndc11
    7247610921
    1 BOTTLE, PLASTIC in 1 CARTON (72476-109-21) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A079174
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "WK2XYI10QM",
    "rxcui": "5640",
    "inchikey": "HEFNNWSXXWATRW-UHFFFAOYSA-N",
    "display_name": "IBUPROFEN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "aeee629b-255c-40d8-8e95-779aec00f723": {
      "match": "brand_token",
      "title": "IBUPROFEN TABLET [NORTHSTAR RX LLC]",
      "spl_version": "1",
      "published_date": "2026-06-02"
    }
  },
  "productid": "72476-109_43e180c4-f363-167e-e063-6394a90ad626",
  "productndc": "72476-109",
  "dosage_form": "TABLET, COATED",
  "orange_book": {
    "appl_no": "079174",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "200MG",
        "product_no": "001",
        "approval_date": "Dec 10, 2010"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "IBUPROFEN",
  "proprietary_name": "Ibuprofen",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA079174",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ibuprofen",
  "start_marketing_date": "20200201",
  "active_numerator_strength": "200"
}

Related drugs

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