advil menstrual pain

Generic: ibuprofen sodium

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

Drug Facts

Product Profile

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

ibuprofen sodium 256 mg/1

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0573-0230
Product ID 0573-0230_5b08a4cf-a90b-42ed-b449-c250cdc0a5f4
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA201803
Listing Expiration 2026-12-31
Marketing Start 2016-06-30

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05730230
Hyphenated Format 0573-0230

Supplemental Identifiers

RxCUI
153008 310965
UNII
RM1CE97Z4N

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 menstrual pain (source: ndc)
Generic Name ibuprofen sodium (source: ndc)
Application Number NDA201803 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 256 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0573-0230-20) / 20 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0573-0230-40) / 40 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (2)

0573-0230-20 1 BOTTLE in 1 CARTON (0573-0230-20) / 20 TABLET, COATED in 1 BOTTLE 0573-0230-40 1 BOTTLE in 1 CARTON (0573-0230-40) / 40 TABLET, COATED in 1 BOTTLE

Ingredients (1)

ibuprofen sodium (256 mg/1)

Linked Drug Pages (1)

Advil Menstrual Pain ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5b08a4cf-a90b-42ed-b449-c250cdc0a5f4", "openfda": {"unii": ["RM1CE97Z4N"], "rxcui": ["153008", "310965"], "spl_set_id": ["ae1625f4-ef32-4d4f-bf54-c44085843e41"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0573-0230-20)  / 20 TABLET, COATED in 1 BOTTLE", "package_ndc": "0573-0230-20", "marketing_start_date": "20160701"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0573-0230-40)  / 40 TABLET, COATED in 1 BOTTLE", "package_ndc": "0573-0230-40", "marketing_start_date": "20160701"}], "brand_name": "Advil Menstrual Pain", "product_id": "0573-0230_5b08a4cf-a90b-42ed-b449-c250cdc0a5f4", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0573-0230", "generic_name": "ibuprofen sodium", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advil Menstrual Pain", "active_ingredients": [{"name": "IBUPROFEN SODIUM", "strength": "256 mg/1"}], "application_number": "NDA201803", "marketing_category": "NDA", "marketing_start_date": "20160630", "listing_expiration_date": "20261231"}