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United States · US · US:49035-604_74e7845e-9b6d-40ba-bb2c-b0a0178ea9c9

equate ibuprofen

Orange BookUNIISPLATC G02CC01

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

Identification

ManufacturerWal-Mart Stores Inc
CountryUS (United States)
ATC codeG02CC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    4903560400
    500 TABLET, FILM COATED in 1 BOTTLE (49035-604-00)
  • ndc11
    4903560405
    2 BOTTLE in 1 PACKAGE (49035-604-05) / 500 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    4903560458
    1 BOTTLE in 1 CARTON (49035-604-58) / 40 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    4903560478
    1 BOTTLE in 1 CARTON (49035-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    4903560482
    2 BOTTLE in 1 CARTON (49035-604-82) / 100 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    4903560485
    1 BOTTLE in 1 CARTON (49035-604-85) / 250 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    4903560490
    2 BOTTLE in 1 PACKAGE (49035-604-90) / 250 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": {
    "2ac53cc7-000f-41fd-b799-4e6d6886fe62": {
      "match": "brand_token",
      "title": "EQUATE DAYTIME COLD AND FLU (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE) SOLUTION [WAL-MART STORES INC]",
      "spl_version": "5",
      "published_date": "2026-06-01"
    }
  },
  "productid": "49035-604_74e7845e-9b6d-40ba-bb2c-b0a0178ea9c9",
  "productndc": "49035-604",
  "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": "equate ibuprofen",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA072096",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ibuprofen",
  "start_marketing_date": "19891015",
  "active_numerator_strength": "200"
}

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