ibuprofen

Generic: ibuprofen

Labeler: marksans pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler marksans pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 800 mg/1

Manufacturer
MARKSANS PHARMA LIMITED

Identifiers & Regulatory

Product NDC 25000-123
Product ID 25000-123_06380458-ba55-458e-b6f8-e6219af48f32
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090796
Listing Expiration 2026-12-31
Marketing Start 2011-02-28

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 25000123
Hyphenated Format 25000-123

Supplemental Identifiers

RxCUI
197805 197806 197807
UPC
0325000121129 0325000123123 0325000122126
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 ANDA090796 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (25000-123-03)
  • 500 TABLET in 1 BOTTLE (25000-123-12)
source: ndc

Packages (2)

25000-123-03 30 TABLET in 1 BOTTLE (25000-123-03) 25000-123-12 500 TABLET in 1 BOTTLE (25000-123-12)

Ingredients (1)

ibuprofen (800 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": "06380458-ba55-458e-b6f8-e6219af48f32", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0325000121129", "0325000123123", "0325000122126"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["e54209c2-f726-440b-ac60-5a72710d2a9b"], "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": ["MARKSANS PHARMA LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (25000-123-03)", "package_ndc": "25000-123-03", "marketing_start_date": "20110228"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (25000-123-12)", "package_ndc": "25000-123-12", "marketing_start_date": "20110228"}], "brand_name": "Ibuprofen", "product_id": "25000-123_06380458-ba55-458e-b6f8-e6219af48f32", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "25000-123", "generic_name": "Ibuprofen", "labeler_name": "MARKSANS PHARMA LIMITED", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20110228", "listing_expiration_date": "20261231"}