all day pain relief

Generic: naproxen sodium

Labeler: valu merchandisers company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

naproxen sodium 220 mg/1

Manufacturer
VALU MERCHANDISERS COMPANY

Identifiers & Regulatory

Product NDC 63941-245
Product ID 63941-245_28729f2d-cd7e-c174-e063-6394a90ac876
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079096
Marketing Start 2010-05-19
Marketing End 2027-09-30

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 63941245
Hyphenated Format 63941-245

Supplemental Identifiers

RxCUI
849574
UPC
0070038577805
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 CARTON (63941-245-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (3)

63941-245-01 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC 63941-245-02 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC 63941-245-03 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-03) / 100 TABLET, COATED 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": "28729f2d-cd7e-c174-e063-6394a90ac876", "openfda": {"upc": ["0070038577805"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["593b915f-045a-40b7-b86e-0d1cb41f2bb8"], "manufacturer_name": ["VALU MERCHANDISERS COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-245-01)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-245-01", "marketing_end_date": "20261130", "marketing_start_date": "20100610"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-245-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-245-02", "marketing_end_date": "20261130", "marketing_start_date": "20100519"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-245-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-245-03", "marketing_end_date": "20270930", "marketing_start_date": "20100519"}], "brand_name": "All Day Pain Relief", "product_id": "63941-245_28729f2d-cd7e-c174-e063-6394a90ac876", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63941-245", "generic_name": "NAPROXEN SODIUM", "labeler_name": "VALU MERCHANDISERS COMPANY", "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_end_date": "20270930", "marketing_start_date": "20100519"}