dual pain reliever

Generic: acetaminophen, ibuprofen

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dual pain reliever
Generic Name acetaminophen, ibuprofen
Labeler walgreen company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 250 mg/1, ibuprofen 125 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-5220
Product ID 0363-5220_f64cb05e-be18-481e-894f-bdc0b8c2ef88
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA214836
Listing Expiration 2026-12-31
Marketing Start 2023-03-10

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 03635220
Hyphenated Format 0363-5220

Supplemental Identifiers

RxCUI
2387532
UNII
362O9ITL9D 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 dual pain reliever (source: ndc)
Generic Name acetaminophen, ibuprofen (source: ndc)
Application Number ANDA214836 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
  • 125 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-5220-01) / 216 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-5220-16) / 144 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-5220-23) / 72 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-5220-68) / 36 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (4)

0363-5220-01 1 BOTTLE in 1 CARTON (0363-5220-01) / 216 TABLET, FILM COATED in 1 BOTTLE 0363-5220-16 1 BOTTLE in 1 CARTON (0363-5220-16) / 144 TABLET, FILM COATED in 1 BOTTLE 0363-5220-23 1 BOTTLE in 1 CARTON (0363-5220-23) / 72 TABLET, FILM COATED in 1 BOTTLE 0363-5220-68 1 BOTTLE in 1 CARTON (0363-5220-68) / 36 TABLET, FILM COATED in 1 BOTTLE

Ingredients (2)

acetaminophen (250 mg/1) ibuprofen (125 mg/1)

Linked Drug Pages (1)

dual pain reliever ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f64cb05e-be18-481e-894f-bdc0b8c2ef88", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["5cb3b0b4-5b47-4ed4-a5e3-f14dbbcb46df"], "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": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5220-01)  / 216 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-5220-01", "marketing_start_date": "20231211"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5220-16)  / 144 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-5220-16", "marketing_start_date": "20231211"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5220-23)  / 72 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-5220-23", "marketing_start_date": "20230310"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5220-68)  / 36 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-5220-68", "marketing_start_date": "20230310"}], "brand_name": "dual pain reliever", "product_id": "0363-5220_f64cb05e-be18-481e-894f-bdc0b8c2ef88", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-5220", "generic_name": "Acetaminophen, Ibuprofen", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dual pain reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA214836", "marketing_category": "ANDA", "marketing_start_date": "20230310", "listing_expiration_date": "20261231"}