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United States · US · US:0363-0945_fafa750f-5cc0-4f13-a808-d63b3d6e7008

Ibuprofen

Orange BookUNIISPLATC G02CC01

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

Identification

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

Packs · 5

  • ndc11
    0363094516
    1 BOTTLE, PLASTIC in 1 BOX (0363-0945-16) / 160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • ndc11
    0363094520
    1 BOTTLE, PLASTIC in 1 BOX (0363-0945-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • ndc11
    0363094530
    300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0363-0945-30)
  • ndc11
    0363094540
    1 BOTTLE, PLASTIC in 1 BOX (0363-0945-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • ndc11
    0363094580
    1 BOTTLE, PLASTIC in 1 BOX (0363-0945-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A206568
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": "0363-0945_fafa750f-5cc0-4f13-a808-d63b3d6e7008",
  "productndc": "0363-0945",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "orange_book": {
    "appl_no": "206568",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 200MG FREE ACID AND POTASSIUM SALT",
        "product_no": "001",
        "approval_date": "Jun 21, 2016"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "IBUPROFEN",
  "proprietary_name": "Ibuprofen",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA206568",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ibuprofen",
  "start_marketing_date": "20180131",
  "active_numerator_strength": "200"
}

Related drugs

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