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United States · US · US:25000-114_1bdc2c02-575f-4b55-ad66-47108f628d18

Ibuprofen

Orange BookUNIISPLATC G02CC01

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

Identification

ManufacturerMARKSANS PHARMA LIMITED
CountryUS (United States)
ATC codeG02CC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 9

  • ndc11
    2500011402
    1 BOTTLE in 1 CARTON (25000-114-02) / 24 TABLET in 1 BOTTLE
  • ndc11
    2500011403
    30 TABLET in 1 BOTTLE (25000-114-03)
  • ndc11
    2500011414
    1000 TABLET in 1 BOTTLE (25000-114-14)
  • ndc11
    2500011420
    4 BAG in 1 BOX (25000-114-20) / 6500 TABLET in 1 BAG
  • ndc11
    2500011430
    6 BAG in 1 BOX (25000-114-30) / 6500 TABLET in 1 BAG
  • ndc11
    2500011470
    500 TABLET in 1 BOTTLE (25000-114-70)
  • ndc11
    2500011471
    1000 TABLET in 1 BOTTLE (25000-114-71)
  • ndc11
    2500011493
    1 BAG in 1 BOX (25000-114-93) / 37470 TABLET in 1 BAG
  • ndc11
    2500011498
    1 BAG in 1 BOX (25000-114-98) / 34065 TABLET in 1 BAG

Annotations

UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A091239
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": "25000-114_1bdc2c02-575f-4b55-ad66-47108f628d18",
  "productndc": "25000-114",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "091239",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "200MG",
        "product_no": "001",
        "approval_date": "Feb 1, 2011"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "IBUPROFEN",
  "proprietary_name": "Ibuprofen",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA091239",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ibuprofen",
  "start_marketing_date": "20110725",
  "active_numerator_strength": "200"
}

Related drugs

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