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United States · US · US:0363-0604_8c0ff9e7-6d01-4bab-b0ca-7779c10d9b77

ibuprofen

Orange BookUNIISPLATC G02CC01

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

Identification

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

Packs · 5

  • ndc11
    0363060462
    1 BOTTLE in 1 CARTON (0363-0604-62) / 24 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    0363060471
    1 BOTTLE in 1 CARTON (0363-0604-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    0363060476
    1 BOTTLE in 1 CARTON (0363-0604-76) / 120 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    0363060478
    1 BOTTLE in 1 CARTON (0363-0604-78) / 100 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    0363060482
    2 BOTTLE in 1 CARTON (0363-0604-82) / 100 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A072096
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": "0363-0604_8c0ff9e7-6d01-4bab-b0ca-7779c10d9b77",
  "productndc": "0363-0604",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "072096",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "200MG",
        "product_no": "001",
        "approval_date": "Dec 8, 1987"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "IBUPROFEN",
  "proprietary_name": "ibuprofen",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA072096",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ibuprofen",
  "start_marketing_date": "20090121",
  "active_numerator_strength": "200"
}

Related drugs

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