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United States · US · US:25000-062_009afd24-3f12-4208-876d-f22ce92a40ce

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 · 7

  • ndc11
    2500006201
    1 BOTTLE in 1 CARTON (25000-062-01) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE
  • ndc11
    2500006204
    1 BOTTLE in 1 CARTON (25000-062-04) / 32 CAPSULE, LIQUID FILLED in 1 BOTTLE
  • ndc11
    2500006213
    600 CAPSULE, LIQUID FILLED in 1 BOTTLE (25000-062-13)
  • ndc11
    2500006243
    1 BOTTLE in 1 CARTON (25000-062-43) / 10 CAPSULE, LIQUID FILLED in 1 BOTTLE
  • ndc11
    2500006267
    1 BOTTLE in 1 CARTON (25000-062-67) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE
  • ndc11
    2500006269
    300 CAPSULE, LIQUID FILLED in 1 BOTTLE (25000-062-69)
  • ndc11
    2500006287
    1 BAG in 1 BOX (25000-062-87) / 2500 CAPSULE, LIQUID FILLED in 1 BAG

Annotations

UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A079205
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": "25000-062_009afd24-3f12-4208-876d-f22ce92a40ce",
  "productndc": "25000-062",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "orange_book": {
    "appl_no": "079205",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 200MG FREE ACID AND POTASSIUM SALT",
        "product_no": "001",
        "approval_date": "Jun 26, 2009"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "IBUPROFEN",
  "proprietary_name": "Ibuprofen",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA079205",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ibuprofen",
  "start_marketing_date": "20200818",
  "active_numerator_strength": "200"
}

Related drugs

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