ibuprofen

Generic: ibuprofen

Labeler: cardinal health 107, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler cardinal health 107, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-0669
Product ID 55154-0669_bab255d0-ad22-4cc3-8a86-351db9ff69e8
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075139
Listing Expiration 2027-12-31
Marketing Start 2011-06-03

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 551540669
Hyphenated Format 55154-0669

Supplemental Identifiers

RxCUI
310965
UPC
0055154066907
UNII
WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

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 ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA075139 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-0669-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bab255d0-ad22-4cc3-8a86-351db9ff69e8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0055154066907"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["260f5862-d65d-4c34-bf53-26ca30806a67"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-0669-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-0669-0", "marketing_start_date": "20110603"}], "brand_name": "Ibuprofen", "product_id": "55154-0669_bab255d0-ad22-4cc3-8a86-351db9ff69e8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "55154-0669", "generic_name": "Ibuprofen", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075139", "marketing_category": "ANDA", "marketing_start_date": "20110603", "listing_expiration_date": "20271231"}