all day pain relief (79903-005)

Drug Facts

Product Profile

Brand Name all day pain relief

Generic Name naproxen sodium

Labeler walmart inc.

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

naproxen sodium 220 mg/1

Manufacturer

WALMART INC.

Identifiers & Regulatory

Product NDC 79903-005

Product ID 79903-005_7ff7ea22-53e8-4895-9960-c48a4bc4ad83

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA204872

Listing Expiration 2026-12-31

Marketing Start 2020-10-22

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 79903005

Hyphenated Format 79903-005

Supplemental Identifiers

RxCUI

849574

UPC

0194346189120

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 ANDA204872 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

220 mg/1

source: ndc

Packaging

200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20)
225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25)
270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90)

source: ndc

Packages (4)

79903-005-20 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20) 79903-005-25 225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25) 79903-005-27 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27) 79903-005-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90)

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": "7ff7ea22-53e8-4895-9960-c48a4bc4ad83", "openfda": {"upc": ["0194346189120"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["c4909e43-57ba-44bc-a234-a02cc884891c"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20)", "package_ndc": "79903-005-20", "marketing_start_date": "20201022"}, {"sample": false, "description": "225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25)", "package_ndc": "79903-005-25", "marketing_start_date": "20201022"}, {"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27)", "package_ndc": "79903-005-27", "marketing_start_date": "20201022"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90)", "package_ndc": "79903-005-90", "marketing_start_date": "20201022"}], "brand_name": "All Day Pain Relief", "product_id": "79903-005_7ff7ea22-53e8-4895-9960-c48a4bc4ad83", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-005", "generic_name": "Naproxen Sodium", "labeler_name": "WALMART INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20201022", "listing_expiration_date": "20261231"}