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United States · US · US:85237-1785_46fe50eb-e432-a593-e063-6294a90a7e1c

Advil Liquigel

Orange BookUNIISPLATC G02CC01

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

Identification

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

Packs · 4

  • ndc11
    8523717851
    1 POUCH in 1 BLISTER PACK (85237-1785-1) / 1 CAPSULE, LIQUID FILLED in 1 POUCH
  • ndc11
    8523717852
    2 POUCH in 1 BLISTER PACK (85237-1785-2) / 2 CAPSULE, LIQUID FILLED in 1 POUCH
  • ndc11
    8523717854
    25 POUCH in 1 BOX, UNIT-DOSE (85237-1785-4) / 2 CAPSULE, LIQUID FILLED in 1 POUCH
  • ndc11
    8523717855
    30 POUCH in 1 BOX, UNIT-DOSE (85237-1785-5) / 2 CAPSULE, LIQUID FILLED in 1 POUCH

Annotations

UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
N020402
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": {
    "a3c30dd2-75f3-4f8b-88d7-4a63dea5bad7": {
      "match": "brand_token",
      "title": "ADVIL PM (DIPHENHYDRAMINE CITRATE, IBUPROFEN) TABLET, COATED [NAVAJO MANUFACTURING COMPANY INC.]",
      "spl_version": "3",
      "published_date": "2026-04-09"
    }
  },
  "productid": "85237-1785_46fe50eb-e432-a593-e063-6294a90a7e1c",
  "productndc": "85237-1785",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "orange_book": {
    "appl_no": "020402",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "EQ 200MG FREE ACID AND POTASSIUM SALT",
        "product_no": "001",
        "approval_date": "Apr 20, 1995"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "EQ 200MG FREE ACID AND POTASSIUM SALT",
        "product_no": "002",
        "approval_date": "Mar 16, 2000"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "IBUPROFEN",
  "proprietary_name": "Advil Liquigel",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA020402",
  "marketing_category": "NDA",
  "nonproprietary_name": "ibuprofen",
  "start_marketing_date": "19950410",
  "active_numerator_strength": "200"
}

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