ibuprofen

Generic: ibuprofen

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler p & l development, llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-139
Product ID 59726-139_c8b9e254-52a0-423e-81b8-b6f503a443b3
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079129
Listing Expiration 2026-12-31
Marketing Start 2024-08-15

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 59726139
Hyphenated Format 59726-139

Supplemental Identifiers

RxCUI
310965
UPC
0359726139502
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 ANDA079129 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 500 TABLET, COATED in 1 BOTTLE, PLASTIC (59726-139-50)
source: ndc

Packages (1)

59726-139-50 500 TABLET, COATED in 1 BOTTLE, PLASTIC (59726-139-50)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c8b9e254-52a0-423e-81b8-b6f503a443b3", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0359726139502"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["6d1c9a64-c83c-4b3d-9245-704b94cb367c"], "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": ["P & L Development, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (59726-139-50)", "package_ndc": "59726-139-50", "marketing_start_date": "20240815"}], "brand_name": "Ibuprofen", "product_id": "59726-139_c8b9e254-52a0-423e-81b8-b6f503a443b3", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "59726-139", "generic_name": "Ibuprofen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079129", "marketing_category": "ANDA", "marketing_start_date": "20240815", "listing_expiration_date": "20261231"}