ibupak
Generic: ibuprofen
Labeler: puretek corporationDrug Facts
Product Profile
Brand Name
ibupak
Generic Name
ibuprofen
Labeler
puretek corporation
Dosage Form
KIT
Routes
Manufacturer
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
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 600 mg
Packaging
- 1 KIT in 1 KIT (59088-756-00) * 100 TABLET, FILM COATED in 1 BOTTLE (67877-320-01)
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"}