ibupak

Generic: ibuprofen

Labeler: puretek corporation
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name ibupak
Generic Name ibuprofen
Labeler puretek corporation
Dosage Form KIT
Routes
ORAL
Manufacturer
PureTek Corporation

Identifiers & Regulatory

Product NDC 59088-756
Product ID 59088-756_f2051c68-cdec-58b2-e053-2995a90a6b48
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2020-05-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59088756
Hyphenated Format 59088-756

Supplemental Identifiers

RxCUI
197806

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ibupak (source: ndc)
Generic Name ibuprofen (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg
source: label
Packaging
  • 1 KIT in 1 KIT (59088-756-00) * 100 TABLET, FILM COATED in 1 BOTTLE (67877-320-01)
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f2051c68-cdec-58b2-e053-2995a90a6b48", "openfda": {"rxcui": ["197806"], "spl_set_id": ["a63f3857-92d1-0adf-e053-2995a90a3afa"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (59088-756-00)  *  100 TABLET, FILM COATED in 1 BOTTLE (67877-320-01)", "package_ndc": "59088-756-00", "marketing_start_date": "20200522"}], "brand_name": "IBUPAK", "product_id": "59088-756_f2051c68-cdec-58b2-e053-2995a90a6b48", "dosage_form": "KIT", "product_ndc": "59088-756", "generic_name": "Ibuprofen", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBUPAK", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20200522", "listing_expiration_date": "20261231"}