leader dual action pain reliever (70000-0737)

Drug Facts

Product Profile

Brand Name leader dual action pain reliever

Generic Name acetaminophen, ibuprofen

Labeler cardinal health 110, llc. dba leader

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

acetaminophen 250 mg/1, ibuprofen 125 mg/1

Manufacturer

Cardinal Health 110, LLC. dba Leader

Identifiers & Regulatory

Product NDC 70000-0737

Product ID 70000-0737_5692f13a-51c6-486c-a57c-b5f99b90aeb9

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA214836

Listing Expiration 2026-12-31

Marketing Start 2025-09-30

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 700000737

Hyphenated Format 70000-0737

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 leader dual action 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 (70000-0737-1) / 18 TABLET, FILM COATED in 1 BOTTLE
1 BOTTLE in 1 CARTON (70000-0737-2) / 36 TABLET, FILM COATED in 1 BOTTLE

source: ndc

Packages (2)

70000-0737-1 1 BOTTLE in 1 CARTON (70000-0737-1) / 18 TABLET, FILM COATED in 1 BOTTLE 70000-0737-2 1 BOTTLE in 1 CARTON (70000-0737-2) / 36 TABLET, FILM COATED in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

Leader Dual Action Pain Reliever ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "5692f13a-51c6-486c-a57c-b5f99b90aeb9", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["2bb1f616-48af-4fe1-9aa9-32fcb2dba50c"], "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": ["Cardinal Health 110, LLC. dba Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0737-1)  / 18 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0737-1", "marketing_start_date": "20250930"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0737-2)  / 36 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0737-2", "marketing_start_date": "20250930"}], "brand_name": "Leader Dual Action Pain Reliever", "product_id": "70000-0737_5692f13a-51c6-486c-a57c-b5f99b90aeb9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70000-0737", "generic_name": "Acetaminophen, Ibuprofen", "labeler_name": "Cardinal Health 110, LLC. dba Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Leader Dual Action 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": "20250930", "listing_expiration_date": "20261231"}