IBUPAK

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

Identification

ManufacturerPureTek Corporation

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5908875600
1 KIT in 1 KIT (59088-756-00) * 100 TABLET, FILM COATED in 1 BOTTLE (67877-320-01)

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Raw payload (JSON)

{
  "route": "ORAL",
  "productid": "59088-756_f2051c68-cdec-58b2-e053-2995a90a6b48",
  "productndc": "59088-756",
  "dosage_form": "KIT",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": null,
  "proprietary_name": "IBUPAK",
  "active_ingred_unit": null,
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Ibuprofen",
  "start_marketing_date": "20200522",
  "active_numerator_strength": null
}

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