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United States · US · US:59556-855_1f4159ad-d58c-4519-932b-030cc2735514

Ibuprofen

Orange BookUNIISPLATC G02CC01

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

Identification

ManufacturerStrides Pharma Inc.
CountryUS (United States)
ATC codeG02CC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    5955685506
    1 BOTTLE in 1 CARTON (59556-855-06) / 100 TABLET, COATED in 1 BOTTLE
  • ndc11
    5955685507
    1 BOTTLE in 1 CARTON (59556-855-07) / 500 TABLET, COATED in 1 BOTTLE
  • ndc11
    5955685508
    1 BOTTLE in 1 CARTON (59556-855-08) / 1000 TABLET, COATED in 1 BOTTLE
  • ndc11
    5955685525
    1 BOTTLE in 1 CARTON (59556-855-25) / 50 TABLET, COATED in 1 BOTTLE
  • ndc11
    5955685541
    1 BOTTLE in 1 CARTON (59556-855-41) / 24 TABLET, COATED in 1 BOTTLE
  • ndc11
    5955685544
    1 BOTTLE in 1 CARTON (59556-855-44) / 165 TABLET, COATED in 1 BOTTLE
  • ndc11
    5955685546
    1000 TABLET, COATED in 1 BAG (59556-855-46)

Annotations

UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A091355
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": "59556-855_1f4159ad-d58c-4519-932b-030cc2735514",
  "productndc": "59556-855",
  "dosage_form": "TABLET, COATED",
  "orange_book": {
    "appl_no": "091355",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "200MG",
        "product_no": "001",
        "approval_date": "Apr 4, 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": "ANDA091355",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ibuprofen",
  "start_marketing_date": "20110404",
  "active_numerator_strength": "200"
}

Related drugs

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