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United States · US · US:41250-604_4e6148c7-fafa-4303-bc95-1dc96dee075d

ibuprofen

Orange BookUNIISPLATC G02CC01

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

Identification

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

Packs · 5

  • ndc11
    4125060462
    1 BOTTLE in 1 CARTON (41250-604-62) / 24 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    4125060471
    1 BOTTLE in 1 CARTON (41250-604-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    4125060478
    1 BOTTLE in 1 CARTON (41250-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    4125060482
    2 BOTTLE in 1 CARTON (41250-604-82) / 100 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    4125060490
    500 TABLET, FILM COATED in 1 BOTTLE (41250-604-90)

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": "41250-604_4e6148c7-fafa-4303-bc95-1dc96dee075d",
  "productndc": "41250-604",
  "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": "19880215",
  "active_numerator_strength": "200"
}

Related drugs

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