Ibuprofen

Orange BookUNIISPLATC G02CC01

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

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
7133510730
84 TABLET, FILM COATED in 1 BOTTLE (71335-1073-0)
ndc11
7133510731
20 TABLET, FILM COATED in 1 BOTTLE (71335-1073-1)
ndc11
7133510732
15 TABLET, FILM COATED in 1 BOTTLE (71335-1073-2)
ndc11
7133510733
40 TABLET, FILM COATED in 1 BOTTLE (71335-1073-3)
ndc11
7133510734
21 TABLET, FILM COATED in 1 BOTTLE (71335-1073-4)
ndc11
7133510735
30 TABLET, FILM COATED in 1 BOTTLE (71335-1073-5)
ndc11
7133510736
90 TABLET, FILM COATED in 1 BOTTLE (71335-1073-6)
ndc11
7133510737
100 TABLET, FILM COATED in 1 BOTTLE (71335-1073-7)
ndc11
7133510738
120 TABLET, FILM COATED in 1 BOTTLE (71335-1073-8)
ndc11
7133510739
60 TABLET, FILM COATED in 1 BOTTLE (71335-1073-9)

Annotations

UNII (FDA Substance ID)

WK2XYI10QM

IBUPROFEN

RxCUI 5640

Orange Book

A091625

ABABAB

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": "71335-1073_b89c7694-78ee-4955-b6fb-faee2398cf98",
  "productndc": "71335-1073",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "091625",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "400MG",
        "product_no": "001",
        "approval_date": "Sep 15, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "600MG",
        "product_no": "002",
        "approval_date": "Sep 15, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "800MG",
        "product_no": "003",
        "approval_date": "Sep 15, 2015"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "IBUPROFEN",
  "proprietary_name": "Ibuprofen",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA091625",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ibuprofen",
  "start_marketing_date": "20151221",
  "active_numerator_strength": "800"
}

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