leader all day pain relief

Generic: naproxen sodium

Labeler: cardinal health 110, llc. dba leader
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name leader all day pain relief
Generic Name naproxen sodium
Labeler cardinal health 110, llc. dba leader
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Cardinal Health 110, LLC. dba Leader

Identifiers & Regulatory

Product NDC 70000-0171
Product ID 70000-0171_b063c471-3082-43b3-8fc5-ece0715c6df4
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074661
Listing Expiration 2027-12-31
Marketing Start 2016-11-29

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 700000171
Hyphenated Format 70000-0171

Supplemental Identifiers

RxCUI
849574
UNII
9TN87S3A3C

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 all day pain relief (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA074661 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (70000-0171-3) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (70000-0171-5) / 24 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (70000-0171-6) / 90 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (3)

70000-0171-3 1 BOTTLE in 1 CARTON (70000-0171-3) / 50 TABLET, FILM COATED in 1 BOTTLE 70000-0171-5 1 BOTTLE in 1 CARTON (70000-0171-5) / 24 TABLET, FILM COATED in 1 BOTTLE 70000-0171-6 1 BOTTLE in 1 CARTON (70000-0171-6) / 90 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Leader All Day Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b063c471-3082-43b3-8fc5-ece0715c6df4", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["dbf007f5-c792-43a7-8cc1-bfa617f3a7fa"], "manufacturer_name": ["Cardinal Health 110, LLC. dba Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0171-3)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0171-3", "marketing_start_date": "20170216"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0171-5)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0171-5", "marketing_start_date": "20210923"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0171-6)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0171-6", "marketing_start_date": "20220524"}], "brand_name": "Leader All Day Pain Relief", "product_id": "70000-0171_b063c471-3082-43b3-8fc5-ece0715c6df4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70000-0171", "generic_name": "Naproxen Sodium", "labeler_name": "Cardinal Health 110, LLC. dba Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Leader All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20161129", "listing_expiration_date": "20271231"}