ibuprofen
Generic: ibuprofen
Labeler: amneal pharmaceuticals llcDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
amneal pharmaceuticals llc
Dosage Form
TABLET
Routes
Active Ingredients
ibuprofen 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
65162-464
Product ID
65162-464_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)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65162464
Hyphenated Format
65162-464
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ibuprofen (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA078558 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (65162-464-03)
- 60 TABLET in 1 BOTTLE (65162-464-06)
- 90 TABLET in 1 BOTTLE (65162-464-09)
- 100 TABLET in 1 BOTTLE (65162-464-10)
- 500 TABLET in 1 BOTTLE (65162-464-50)
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
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 (65162-464-03)", "package_ndc": "65162-464-03", "marketing_start_date": "20091123"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (65162-464-06)", "package_ndc": "65162-464-06", "marketing_start_date": "20091123"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65162-464-09)", "package_ndc": "65162-464-09", "marketing_start_date": "20091123"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-464-10)", "package_ndc": "65162-464-10", "marketing_start_date": "20091123"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-464-50)", "package_ndc": "65162-464-50", "marketing_start_date": "20091123"}], "brand_name": "Ibuprofen", "product_id": "65162-464_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": "65162-464", "generic_name": "Ibuprofen", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "400 mg/1"}], "application_number": "ANDA078558", "marketing_category": "ANDA", "marketing_start_date": "20091123", "listing_expiration_date": "20261231"}