ibuprofen

Generic: ibuprofen

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 800 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-556
Product ID 72189-556_4c4c7dc3-d5c8-f3d9-e063-6294a90a426f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213794
Listing Expiration 2027-12-31
Marketing Start 2024-06-11

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 72189556
Hyphenated Format 72189-556

Supplemental Identifiers

RxCUI
197807
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 ANDA213794 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (72189-556-20)
  • 21 TABLET in 1 BOTTLE (72189-556-21)
  • 30 TABLET in 1 BOTTLE (72189-556-30)
  • 40 TABLET in 1 BOTTLE (72189-556-40)
  • 45 TABLET in 1 BOTTLE (72189-556-45)
  • 60 TABLET in 1 BOTTLE (72189-556-60)
  • 100 TABLET in 1 BOTTLE (72189-556-71)
  • 90 TABLET in 1 BOTTLE (72189-556-90)
source: ndc

Packages (8)

72189-556-20 20 TABLET in 1 BOTTLE (72189-556-20) 72189-556-21 21 TABLET in 1 BOTTLE (72189-556-21) 72189-556-30 30 TABLET in 1 BOTTLE (72189-556-30) 72189-556-40 40 TABLET in 1 BOTTLE (72189-556-40) 72189-556-45 45 TABLET in 1 BOTTLE (72189-556-45) 72189-556-60 60 TABLET in 1 BOTTLE (72189-556-60) 72189-556-71 100 TABLET in 1 BOTTLE (72189-556-71) 72189-556-90 90 TABLET in 1 BOTTLE (72189-556-90)

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": "4c4c7dc3-d5c8-f3d9-e063-6294a90a426f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["1aa11b52-1aca-9219-e063-6294a90a470f"], "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": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (72189-556-20)", "package_ndc": "72189-556-20", "marketing_start_date": "20240611"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (72189-556-21)", "package_ndc": "72189-556-21", "marketing_start_date": "20240611"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-556-30)", "package_ndc": "72189-556-30", "marketing_start_date": "20240611"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (72189-556-40)", "package_ndc": "72189-556-40", "marketing_start_date": "20240611"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (72189-556-45)", "package_ndc": "72189-556-45", "marketing_start_date": "20240611"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-556-60)", "package_ndc": "72189-556-60", "marketing_start_date": "20240611"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72189-556-71)", "package_ndc": "72189-556-71", "marketing_start_date": "20240611"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-556-90)", "package_ndc": "72189-556-90", "marketing_start_date": "20240611"}], "brand_name": "Ibuprofen", "product_id": "72189-556_4c4c7dc3-d5c8-f3d9-e063-6294a90a426f", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72189-556", "generic_name": "Ibuprofen", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA213794", "marketing_category": "ANDA", "marketing_start_date": "20240611", "listing_expiration_date": "20271231"}