all day pain relief

Generic: naproxen sodium

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day pain relief
Generic Name naproxen sodium
Labeler walgreen company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 200 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-0938
Product ID 0363-0938_020d7f84-045c-47f3-88f9-b153a6d43ab2
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074661
Listing Expiration 2026-12-31
Marketing Start 2014-07-31

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 03630938
Hyphenated Format 0363-0938

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

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 200 TABLET, FILM COATED in 1 BOTTLE (0363-0938-82)
source: ndc

Packages (1)

0363-0938-82 200 TABLET, FILM COATED in 1 BOTTLE (0363-0938-82)

Ingredients (1)

naproxen sodium (200 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": "020d7f84-045c-47f3-88f9-b153a6d43ab2", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["8ea540bf-4958-41f9-980f-5936c074a51d"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE (0363-0938-82)", "package_ndc": "0363-0938-82", "marketing_start_date": "20140731"}], "brand_name": "all day pain relief", "product_id": "0363-0938_020d7f84-045c-47f3-88f9-b153a6d43ab2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-0938", "generic_name": "Naproxen Sodium", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "all day pain relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "200 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20140731", "listing_expiration_date": "20261231"}