FDA.reportPublic FDA data

All Day Pain Relief

Product NDC
63941-144
11-digit product format
639410144
Labeler code
63941
Product ID
63941-144_28728294-39fb-8c0b-e063-6394a90a95c2
Type
HUMAN OTC DRUG
Nonproprietary name
NAPROXEN SODIUM
Dosage form
TABLET, COATED
Route
ORAL
Labeler
VALU MERCHANDISERS COMPANY
Application
ANDA079096
Marketing category
ANDA
Marketing start
2010-06-10
Marketing end
2026-10-31
Substance
NAPROXEN SODIUM
Active strength
220 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
All Day Pain Relief

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NAPROXEN SODIUM220 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9TN87S3A3C
Rxcui849574

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fef6ad89-235f-4274-ba49-a8e53642473eProduct name220250225
87fed3e6-8fba-48ef-96b0-3a7fb54b96ffProduct name320230306
b5fdaaec-7251-4da6-9cb2-4e9e76939ec8Product name120200623
e76dbbc1-775d-722c-08ff-ed45e8a80defProduct name320181002
6f4f4521-fd56-1ae6-888b-3b021bd75c7cProduct name120140508
ce67e27d-1d21-5465-4409-b0662dd99d4dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63941-144-01All Day Pain Relief1 in 1 CARTONTABLET, COATED13
63941-144-01All Day Pain Relief24 in 1 BOTTLE, PLASTICTABLET, COATED243
63941-144-02All Day Pain Relief50 in 1 BOTTLE, PLASTICTABLET, COATED503
63941-144-02All Day Pain Relief1 in 1 CARTONTABLET, COATED13
63941-144-03All Day Pain Relief100 in 1 BOTTLE, PLASTICTABLET, COATED1003
63941-144-03All Day Pain Relief1 in 1 CARTONTABLET, COATED13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63941-144ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, COATED [VALU MERCHANDISERS COMPANY]3Current NDC, Legacy NDC, 6 package rows20241206_48059718-4e35-479c-a549-ac534d3ba899.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
849574naproxen sodium 220 MG Oral TabletPSN48059718-4e35-479c-a549-ac534d3ba8993
849574naproxen sodium 220 MG Oral TabletSCD48059718-4e35-479c-a549-ac534d3ba8993
849574naproxen sodium 220 MG (as naproxen 200 MG) Oral TabletSY48059718-4e35-479c-a549-ac534d3ba8993

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63941-144-01639410144011 BOTTLE, PLASTIC in 1 CARTON (63941-144-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC2010-06-292026-10-31NoNoCurrent
63941-144-02639410144021 BOTTLE, PLASTIC in 1 CARTON (63941-144-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC2010-06-102026-10-31NoNoCurrent
63941-144-03639410144031 BOTTLE, PLASTIC in 1 CARTON (63941-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC2010-08-032026-10-31NoNoCurrent