ibuprofen

Generic: ibuprofen

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 600 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-895
Product ID 71610-895_31f59302-eaf0-211b-e063-6294a90a08b0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078329
Listing Expiration 2026-12-31
Marketing Start 2018-08-24

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 71610895
Hyphenated Format 71610-895

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 ANDA078329 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (71610-895-60)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71610-895-70)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71610-895-80)
  • 270 TABLET, FILM COATED in 1 BOTTLE (71610-895-92)
source: ndc

Packages (4)

71610-895-60 90 TABLET, FILM COATED in 1 BOTTLE (71610-895-60) 71610-895-70 120 TABLET, FILM COATED in 1 BOTTLE (71610-895-70) 71610-895-80 180 TABLET, FILM COATED in 1 BOTTLE (71610-895-80) 71610-895-92 270 TABLET, FILM COATED in 1 BOTTLE (71610-895-92)

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": "31f59302-eaf0-211b-e063-6294a90a08b0", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["31f59d10-d821-2291-e063-6294a90ac518"], "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": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-895-60)", "package_ndc": "71610-895-60", "marketing_start_date": "20250401"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71610-895-70)", "package_ndc": "71610-895-70", "marketing_start_date": "20250401"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71610-895-80)", "package_ndc": "71610-895-80", "marketing_start_date": "20250401"}, {"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (71610-895-92)", "package_ndc": "71610-895-92", "marketing_start_date": "20250401"}], "brand_name": "Ibuprofen", "product_id": "71610-895_31f59302-eaf0-211b-e063-6294a90a08b0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71610-895", "generic_name": "Ibuprofen", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20180824", "listing_expiration_date": "20261231"}