dual back pain reliever

Generic: acetaminophen, ibuprofen

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

Drug Facts

Product Profile

Brand Name dual back 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 0363-6199
Product ID 0363-6199_3756a89e-f886-4dae-b5b9-896cf53166b3
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA214836
Listing Expiration 2026-12-31
Marketing Start 2024-02-16

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 03636199
Hyphenated Format 0363-6199

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 back 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 (0363-6199-23) / 72 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3756a89e-f886-4dae-b5b9-896cf53166b3", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["9831f374-658a-47ec-8a7e-4ff8359570be"], "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 (0363-6199-23)  / 72 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-6199-23", "marketing_start_date": "20240216"}], "brand_name": "Dual Back Pain Reliever", "product_id": "0363-6199_3756a89e-f886-4dae-b5b9-896cf53166b3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-6199", "generic_name": "acetaminophen, ibuprofen", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dual Back 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": "20240216", "listing_expiration_date": "20261231"}