dual back pain reliever
Generic: acetaminophen, ibuprofen
Labeler: walgreen companyDrug Facts
Product Profile
Brand Name
dual back pain reliever
Generic Name
acetaminophen, ibuprofen
Labeler
walgreen company
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
acetaminophen 250 mg/1, ibuprofen 125 mg/1
Manufacturer
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)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03636199
Hyphenated Format
0363-6199
Supplemental Identifiers
RxCUI
UNII
NUI
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
dual back pain reliever (source: ndc)
Generic Name
acetaminophen, ibuprofen (source: ndc)
Application Number
ANDA214836 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
- 125 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (0363-6199-23) / 72 TABLET, FILM COATED in 1 BOTTLE
Packages (1)
Ingredients (2)
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"}