advil

Generic: ibuprofen

Labeler: haleon us holdings llc
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name advil
Generic Name ibuprofen
Labeler haleon us holdings llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0573-0161
Product ID 0573-0161_2ceac3cb-8f4c-4cd7-bba9-aa9aa0641721
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA018989
Listing Expiration 2026-12-31
Marketing Start 1984-05-18

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 05730161
Hyphenated Format 0573-0161

Supplemental Identifiers

RxCUI
153008 310965
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 advil (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number NDA018989 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0573-0161-35) / 150 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0573-0161-51) / 200 TABLET, COATED in 1 BOTTLE
  • 65 TABLET, COATED in 1 BOTTLE (0573-0161-65)
  • 1 BOTTLE in 1 CARTON (0573-0161-85) / 225 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (4)

0573-0161-35 1 BOTTLE in 1 CARTON (0573-0161-35) / 150 TABLET, COATED in 1 BOTTLE 0573-0161-51 1 BOTTLE in 1 CARTON (0573-0161-51) / 200 TABLET, COATED in 1 BOTTLE 0573-0161-65 65 TABLET, COATED in 1 BOTTLE (0573-0161-65) 0573-0161-85 1 BOTTLE in 1 CARTON (0573-0161-85) / 225 TABLET, COATED in 1 BOTTLE

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

ADVIL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2ceac3cb-8f4c-4cd7-bba9-aa9aa0641721", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["153008", "310965"], "spl_set_id": ["1a665e64-9f30-be37-4a83-38789f1f1e89"], "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": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0573-0161-35)  / 150 TABLET, COATED in 1 BOTTLE", "package_ndc": "0573-0161-35", "marketing_start_date": "19840518"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0573-0161-51)  / 200 TABLET, COATED in 1 BOTTLE", "package_ndc": "0573-0161-51", "marketing_start_date": "19840518"}, {"sample": false, "description": "65 TABLET, COATED in 1 BOTTLE (0573-0161-65)", "package_ndc": "0573-0161-65", "marketing_start_date": "20170501"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0573-0161-85)  / 225 TABLET, COATED in 1 BOTTLE", "package_ndc": "0573-0161-85", "marketing_start_date": "19840518"}], "brand_name": "ADVIL", "product_id": "0573-0161_2ceac3cb-8f4c-4cd7-bba9-aa9aa0641721", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0573-0161", "generic_name": "ibuprofen", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ADVIL", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "NDA018989", "marketing_category": "NDA", "marketing_start_date": "19840518", "listing_expiration_date": "20261231"}