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United States · US · US:62207-321_44a726e4-0a4b-b303-e063-6394a90a9073

IBUPROFEN

Orange BookUNIISPLATC G02CC01

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

Identification

ManufacturerGranules India Limited
CountryUS (United States)
ATC codeG02CC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    6220732141
    24 TABLET in 1 BOTTLE (62207-321-41)
  • ndc11
    6220732142
    50 TABLET in 1 BOTTLE (62207-321-42)
  • ndc11
    6220732143
    100 TABLET in 1 BOTTLE (62207-321-43)
  • ndc11
    6220732146
    250 TABLET in 1 BOTTLE (62207-321-46)
  • ndc11
    6220732147
    500 TABLET in 1 BOTTLE (62207-321-47)
  • ndc11
    6220732148
    750 TABLET in 1 BOTTLE (62207-321-48)
  • ndc11
    6220732149
    1000 TABLET in 1 BOTTLE (62207-321-49)
  • ndc11
    6220732189
    10 TABLET in 1 BOTTLE (62207-321-89)
  • ndc11
    6220732190
    1700 TABLET in 1 BOTTLE (62207-321-90)
  • ndc11
    6220732191
    160000 TABLET in 1 DRUM (62207-321-91)

Annotations

UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A202312
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": "62207-321_44a726e4-0a4b-b303-e063-6394a90a9073",
  "productndc": "62207-321",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "202312",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "200MG",
        "product_no": "001",
        "approval_date": "Oct 7, 2016"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "IBUPROFEN",
  "proprietary_name": "IBUPROFEN",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA202312",
  "marketing_category": "ANDA",
  "nonproprietary_name": "IBUPROFEN",
  "start_marketing_date": "20191114",
  "active_numerator_strength": "200"
}

Related drugs

Other records sharing ATC code G02CC01.

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