ibuprofen

Generic: ibuprofen

Labeler: advanced rx pharmacy of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler advanced rx pharmacy of tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 600 mg/1

Manufacturer
Advanced Rx Pharmacy of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0154
Product ID 80425-0154_2a99a80e-d06d-27e6-e063-6294a90ae0fe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091625
Listing Expiration 2026-12-31
Marketing Start 2015-12-21

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 804250154
Hyphenated Format 80425-0154

Supplemental Identifiers

RxCUI
197806
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 ANDA091625 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (80425-0154-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (80425-0154-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (80425-0154-3)
  • 100 TABLET, FILM COATED in 1 BOTTLE (80425-0154-4)
source: ndc

Packages (4)

80425-0154-1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0154-1) 80425-0154-2 60 TABLET, FILM COATED in 1 BOTTLE (80425-0154-2) 80425-0154-3 90 TABLET, FILM COATED in 1 BOTTLE (80425-0154-3) 80425-0154-4 100 TABLET, FILM COATED in 1 BOTTLE (80425-0154-4)

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": "2a99a80e-d06d-27e6-e063-6294a90ae0fe", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["c859cc7a-e13a-7df4-e053-2a95a90a47d6"], "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": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0154-1)", "package_ndc": "80425-0154-1", "marketing_start_date": "20151221"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0154-2)", "package_ndc": "80425-0154-2", "marketing_start_date": "20151221"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0154-3)", "package_ndc": "80425-0154-3", "marketing_start_date": "20151221"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (80425-0154-4)", "package_ndc": "80425-0154-4", "marketing_start_date": "20230516"}], "brand_name": "Ibuprofen", "product_id": "80425-0154_2a99a80e-d06d-27e6-e063-6294a90ae0fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0154", "generic_name": "Ibuprofen", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA091625", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}