FDA.reportPublic FDA data

All Day Back and Muscle Pain Relief

Product NDC
79903-609
11-digit product format
799030609
Labeler code
79903
Product ID
79903-609_0bafa4ac-8c2d-006b-e063-6294a90ab1fc
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen sodium
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Walmart Inc.
Application
ANDA090545
Marketing category
ANDA
Marketing start
2023-12-15
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
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
All Day Back and Muscle Pain Relief
Listing expiration
2026-12-31

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
79903-609-09All Day Back and Muscle Pain Relief1 in 1 CARTONTABLET, COATED12
79903-609-09All Day Back and Muscle Pain Relief90 in 1 BOTTLETABLET, COATED902
79903-609-20All Day Back and Muscle Pain Relief1 in 1 CARTONTABLET, COATED12
79903-609-20All Day Back and Muscle Pain Relief200 in 1 BOTTLETABLET, COATED2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79903-609ALL DAY BACK AND MUSCLE PAIN RELIEF (NAPROXEN SODIUM) TABLET, COATED [WALMART INC.]2Current NDC, 4 package rows20231215_062b9ffe-b4fc-9f5a-e063-6294a90a560e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
849574naproxen sodium 220 MG Oral TabletPSN062b9ffe-b4fc-9f5a-e063-6294a90a560e2
849574naproxen sodium 220 MG Oral TabletSCD062b9ffe-b4fc-9f5a-e063-6294a90a560e2
849574naproxen sodium 220 MG (as naproxen 200 MG) Oral TabletSY062b9ffe-b4fc-9f5a-e063-6294a90a560e2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
79903-609-09799030609091 BOTTLE in 1 CARTON (79903-609-09) / 90 TABLET, COATED in 1 BOTTLE1 bottle2023-12-15NoNoCurrent
79903-609-20799030609201 BOTTLE in 1 CARTON (79903-609-20) / 200 TABLET, COATED in 1 BOTTLE1 bottle2023-12-15NoNoCurrent