ibuprofen

Generic: ibuprofen

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler amneal pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 600 mg/1

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 65162-465
Product ID 65162-465_32c8853c-ed52-4791-9350-ab724724d342
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078558
Listing Expiration 2026-12-31
Marketing Start 2009-11-23

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 65162465
Hyphenated Format 65162-465

Supplemental Identifiers

RxCUI
197805 197806 197807
UPC
0365162464030 0365162465037 0365162466034
UNII
WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

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 ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA078558 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (65162-465-03)
  • 50 TABLET in 1 BOTTLE (65162-465-05)
  • 60 TABLET in 1 BOTTLE (65162-465-06)
  • 90 TABLET in 1 BOTTLE (65162-465-09)
  • 100 TABLET in 1 BOTTLE (65162-465-10)
  • 500 TABLET in 1 BOTTLE (65162-465-50)
source: ndc

Packages (6)

65162-465-03 30 TABLET in 1 BOTTLE (65162-465-03) 65162-465-05 50 TABLET in 1 BOTTLE (65162-465-05) 65162-465-06 60 TABLET in 1 BOTTLE (65162-465-06) 65162-465-09 90 TABLET in 1 BOTTLE (65162-465-09) 65162-465-10 100 TABLET in 1 BOTTLE (65162-465-10) 65162-465-50 500 TABLET in 1 BOTTLE (65162-465-50)

Ingredients (1)

ibuprofen (600 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": "32c8853c-ed52-4791-9350-ab724724d342", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0365162464030", "0365162465037", "0365162466034"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["17577b3b-e755-45d1-8b53-775d058578b2"], "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": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (65162-465-03)", "package_ndc": "65162-465-03", "marketing_start_date": "20091123"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (65162-465-05)", "package_ndc": "65162-465-05", "marketing_start_date": "20091123"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (65162-465-06)", "package_ndc": "65162-465-06", "marketing_start_date": "20091123"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65162-465-09)", "package_ndc": "65162-465-09", "marketing_start_date": "20091123"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-465-10)", "package_ndc": "65162-465-10", "marketing_start_date": "20091123"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-465-50)", "package_ndc": "65162-465-50", "marketing_start_date": "20091123"}], "brand_name": "Ibuprofen", "product_id": "65162-465_32c8853c-ed52-4791-9350-ab724724d342", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "65162-465", "generic_name": "Ibuprofen", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA078558", "marketing_category": "ANDA", "marketing_start_date": "20091123", "listing_expiration_date": "20261231"}