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 · 9

ndc11
7133506901
20 TABLET, FILM COATED in 1 BOTTLE (71335-0690-1)
ndc11
7133506902
30 TABLET, FILM COATED in 1 BOTTLE (71335-0690-2)
ndc11
7133506903
40 TABLET, FILM COATED in 1 BOTTLE (71335-0690-3)
ndc11
7133506904
60 TABLET, FILM COATED in 1 BOTTLE (71335-0690-4)
ndc11
7133506905
90 TABLET, FILM COATED in 1 BOTTLE (71335-0690-5)
ndc11
7133506906
120 TABLET, FILM COATED in 1 BOTTLE (71335-0690-6)
ndc11
7133506907
100 TABLET, FILM COATED in 1 BOTTLE (71335-0690-7)
ndc11
7133506908
21 TABLET, FILM COATED in 1 BOTTLE (71335-0690-8)
ndc11
7133506909
15 TABLET, FILM COATED in 1 BOTTLE (71335-0690-9)

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": "71335-0690_2f612a58-8c48-4d8a-9819-6e2bca3934cc",
  "productndc": "71335-0690",
  "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": "400"
}

Related drugs

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