advil
Generic: ibuprofen sodium
Labeler: haleon us holdings llcDrug Facts
Product Profile
Brand Name
advil
Generic Name
ibuprofen sodium
Labeler
haleon us holdings llc
Dosage Form
TABLET, COATED
Routes
Active Ingredients
ibuprofen sodium 256 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0573-0134
Product ID
0573-0134_40429ef4-846a-eb4c-e063-6394a90ab7a9
Product Type
HUMAN OTC DRUG
Marketing Category
NDA
Application Number
NDA201803
Listing Expiration
2026-12-31
Marketing Start
2013-07-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05730134
Hyphenated Format
0573-0134
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 sodium (source: ndc)
Application Number
NDA201803 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 256 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (0573-0134-20) / 20 TABLET, COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (0573-0134-80) / 80 TABLET, COATED in 1 BOTTLE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40429ef4-846a-eb4c-e063-6394a90ab7a9", "openfda": {"unii": ["RM1CE97Z4N"], "rxcui": ["153008", "310965"], "spl_set_id": ["5be198b8-396e-4b44-8819-e2e3b5d2ad0e"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0573-0134-20) / 20 TABLET, COATED in 1 BOTTLE", "package_ndc": "0573-0134-20", "marketing_start_date": "20130708"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0573-0134-80) / 80 TABLET, COATED in 1 BOTTLE", "package_ndc": "0573-0134-80", "marketing_start_date": "20130708"}], "brand_name": "Advil", "product_id": "0573-0134_40429ef4-846a-eb4c-e063-6394a90ab7a9", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0573-0134", "generic_name": "ibuprofen sodium", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advil", "active_ingredients": [{"name": "IBUPROFEN SODIUM", "strength": "256 mg/1"}], "application_number": "NDA201803", "marketing_category": "NDA", "marketing_start_date": "20130708", "listing_expiration_date": "20261231"}