all day pain relief

Generic: naproxen sodium

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day pain relief
Generic Name naproxen sodium
Labeler p & l development, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-169
Product ID 59726-169_4f58c6a0-3f3c-42b6-a35b-d0d31c574ec8
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079096
Listing Expiration 2026-12-31
Marketing Start 2014-02-28

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 59726169
Hyphenated Format 59726-169

Supplemental Identifiers

RxCUI
849574
UPC
0359726169400
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 all day pain relief (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA079096 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (59726-169-15) / 15 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 BOX (59726-169-40) / 40 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

59726-169-15 1 BOTTLE, PLASTIC in 1 BOX (59726-169-15) / 15 TABLET in 1 BOTTLE, PLASTIC 59726-169-40 1 BOTTLE, PLASTIC in 1 BOX (59726-169-40) / 40 TABLET in 1 BOTTLE, PLASTIC

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

All Day Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4f58c6a0-3f3c-42b6-a35b-d0d31c574ec8", "openfda": {"upc": ["0359726169400"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["7360ae72-3714-402b-96f1-64dc056bafb8"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-169-15)  / 15 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-169-15", "marketing_start_date": "20140228"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-169-40)  / 40 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-169-40", "marketing_start_date": "20140228"}], "brand_name": "All Day Pain Relief", "product_id": "59726-169_4f58c6a0-3f3c-42b6-a35b-d0d31c574ec8", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "59726-169", "generic_name": "Naproxen sodium", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_start_date": "20140228", "listing_expiration_date": "20261231"}