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United States · US · US:69842-643_d30216c5-0fc3-4812-94f2-0b0e8da4381e

Ibuprofen minis

Orange BookUNIISPLATC G02CC01

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

Identification

ManufacturerCVS Pharmacy
CountryUS (United States)
ATC codeG02CC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    6984264302
    1 BOTTLE, PLASTIC in 1 BOX (69842-643-02) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • ndc11
    6984264316
    1 BOTTLE, PLASTIC in 1 BOX (69842-643-16) / 160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • ndc11
    6984264320
    200 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (69842-643-20)
  • ndc11
    6984264324
    1 BOTTLE, PLASTIC in 1 BOX (69842-643-24) / 24 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • ndc11
    6984264350
    500 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (69842-643-50)
  • ndc11
    6984264380
    1 BOTTLE, PLASTIC in 1 BOX (69842-643-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • ndc11
    6984264388
    1 BOTTLE, PLASTIC in 1 BOX (69842-643-88) / 88 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A206568
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": "69842-643_d30216c5-0fc3-4812-94f2-0b0e8da4381e",
  "productndc": "69842-643",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "orange_book": {
    "appl_no": "206568",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 200MG FREE ACID AND POTASSIUM SALT",
        "product_no": "001",
        "approval_date": "Jun 21, 2016"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "IBUPROFEN",
  "proprietary_name": "Ibuprofen minis",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA206568",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ibuprofen",
  "start_marketing_date": "20181231",
  "active_numerator_strength": "200"
}

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