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United States · US · US:71335-2068_2c91e959-d2c7-48ce-a4a5-6c540fb90895

ibuprofen

Orange BookUNIISPLATC G02CC01

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeG02CC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133520680
    90 TABLET, FILM COATED in 1 BOTTLE (71335-2068-0)
  • ndc11
    7133520681
    20 TABLET, FILM COATED in 1 BOTTLE (71335-2068-1)
  • ndc11
    7133520682
    15 TABLET, FILM COATED in 1 BOTTLE (71335-2068-2)
  • ndc11
    7133520683
    30 TABLET, FILM COATED in 1 BOTTLE (71335-2068-3)
  • ndc11
    7133520684
    100 TABLET, FILM COATED in 1 BOTTLE (71335-2068-4)
  • ndc11
    7133520685
    60 TABLET, FILM COATED in 1 BOTTLE (71335-2068-5)
  • ndc11
    7133520686
    50 TABLET, FILM COATED in 1 BOTTLE (71335-2068-6)
  • ndc11
    7133520687
    40 TABLET, FILM COATED in 1 BOTTLE (71335-2068-7)
  • ndc11
    7133520688
    10 TABLET, FILM COATED in 1 BOTTLE (71335-2068-8)
  • ndc11
    7133520689
    56 TABLET, FILM COATED in 1 BOTTLE (71335-2068-9)

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": "71335-2068_2c91e959-d2c7-48ce-a4a5-6c540fb90895",
  "productndc": "71335-2068",
  "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": "19940816",
  "active_numerator_strength": "200"
}

Related drugs

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