Naproxen Sodium

Product NDC
63187-596
11-digit product format
631870596
Labeler code
63187
Product ID
63187-596_056f2617-2de4-4296-bd4d-714f34f7a15c
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen Sodium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA074661
Marketing category
ANDA
Marketing start
2014-04-11
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
2027-12-31
Current FDA listing
Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A074661-001NAPROXEN SODIUMNAPROXEN SODIUM220MGTABLET / ORAL1997-01-13

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-1384e616aacf4f…
2026-08-18 06:07:402026-07A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-1331067a03dcf5…
2025-08-23 18:47 UTC2025-08A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-136a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-1303ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-132680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-135bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-1379d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-131e350fbaab3a…
2024-05-31 18:47 UTC2024-05A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-138072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-135c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-135d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-134b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-1374a2ff9319b5…
2022-03-09 01:35 UTC2022-03A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-1387673890dc5c…
2021-03-12 10:30 UTC2021-03A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-135aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-138869cabd3fbd…
2020-11-12 02:37 UTC2020-11A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13c0c555d07b60…
2019-12-14 00:12 UTC2019-12A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-133f01610625f2…
2019-09-15 20:21 UTC2019-09A074661-001NAPROXEN SODIUMEQ 200MG BASETABLET / ORAL1997-01-13b00525d2431f…
2019-07-19 19:46 UTC2019-07A074661-001NAPROXEN SODIUMEQ 200MG BASETABLET / ORAL1997-01-13ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-136a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-131c564ffb4f44…
2023-12-20 04:57 UTC2023-12A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-139b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-133f0d92c62455…
2023-05-13 08:27 UTC2023-05A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13053a50430f4f…
2023-01-26 05:58 UTC2023-01A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-133bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-133a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A074661-001NAPROXEN SODIUM220MGTABLET / ORAL1997-01-13f41ea6bd6efb…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Naproxen Sodium
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NAPROXEN SODIUM220 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9TN87S3A3CInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
849574Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
e668c80f-dd53-4b82-8678-5e4fccb13023Available on FDA.report

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
63187-596-24Naproxen Sodium24 in 1 BOTTLETABLET, FILM COATED246
63187-596-28Naproxen Sodium28 in 1 BOTTLETABLET, FILM COATED286
63187-596-30Naproxen Sodium30 in 1 BOTTLETABLET, FILM COATED306
63187-596-60Naproxen Sodium90 in 1 BOTTLETABLET, FILM COATED906
63187-596-90Naproxen Sodium60 in 1 BOTTLETABLET, FILM COATED606

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63187-596-24EA - Each63187-596e3df9d6e-5bce-4060-8041-0986f897063e12017-11-06
63187-596-28EA - Each63187-596e7a3ee7b-799d-4cbb-aade-a7af4c95206812017-10-13
63187-596-30EA - Each63187-596599f0bf3-acc8-4744-a96b-4824ea0d410e12016-04-04

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63187-596NAPROXEN SODIUM TABLET, FILM COATED [PROFICIENT RX LP]6Current NDC, Legacy NDC, 5 package rows20220514_e668c80f-dd53-4b82-8678-5e4fccb13023.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 2 of 3 · 56 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
signature care naproxen sodiumNAPROXEN SODIUMSafeway85f78e63-98aa-4cf3-887d-0ac535184f972025-12-16WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
up and up naproxen sodiumNAPROXEN SODIUMTarget Corporationb0e98603-94e9-474a-88a0-22042f4612712025-11-19WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
up and up naproxen sodiumNAPROXEN SODIUMTarget Corporation00bd8490-f280-4336-b13d-0e11c0bf45862025-11-04WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
Rugby All Day ReliefNAPROXEN SODIUMRugby Laboratories16e107f0-45a3-428f-b849-0f20a848a6022025-10-30WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
Leader All Day Pain ReliefNAPROXEN SODIUMCardinal Health 110, LLC. dba Leaderb01c2b4e-a092-42dc-a387-d181d8ba14bb2025-10-30WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
foster and thrive all day pain reliefNAPROXEN SODIUMStrategic Sourcing Services LLC01746bb6-4068-4737-ba38-04cd5f1a81ba2025-09-12WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
Good Sense Naproxen SodiumNAPROXEN SODIUMBryant Ranch Prepacke5e8768d-c6e0-4018-b788-5ce86929f7b02025-08-26WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
NAPROXEN SODIUMNAPROXEN SODIUMSafeway396f4e60-3dde-433f-b4b5-25f351c96d572025-08-19WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
TopCare All Day Pain ReliefNAPROXEN SODIUMTopco Associates LLC079eccdd-33bd-4b5c-bf46-9aef785590822025-07-22WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
kirkland signature naproxen sodiumNAPROXEN SODIUMCostco Wholesale Companyd63cd2ad-18cf-4379-b48e-a487334ad9cc2025-07-16WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
equaline naproxen sodiumNAPROXEN SODIUMUnited Natural Foods, Inc. dba UNFI1022d075-9bdf-46df-81ac-c84cb26081952025-06-04WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
naproxen sodiumNAPROXEN SODIUMMeijer Distribution Inc72f461bc-621e-4e2b-b437-53a580125f3c2025-05-02WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
basic care naproxen sodiumNAPROXEN SODIUMAmazon.com Services LLC29fc5a16-49ed-41ca-a296-bee34d1d12f62025-04-17WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
Naproxen SodiumNAPROXEN SODIUMBryant Ranch Prepack3d57ba5c-3a1d-435a-aa4f-9cc709e1b8cf2025-03-28WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
rugby all day reliefNAPROXEN SODIUMA-S Medication Solutions369f5123-283d-4aa6-8861-8d183f2ba94d2025-03-18WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
Care One Naproxen SodiumNAPROXEN SODIUMAmerican Sales Company88812af7-89ca-449b-9513-20c284543d0e2025-03-13WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
CareOne Naproxen SodiumNAPROXEN SODIUMAmerican Sales Company0ac4c343-a5b6-4f69-a75a-87074dc867e82025-03-04WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
Naproxen SodiumNAPROXEN SODIUMMeijer Distribution Inc9551e84b-19bc-43e7-9c6e-0f24fdeb5abe2025-03-03WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
All Day ReliefNAPROXEN SODIUMPublix Super Markets Inc688451a2-e94a-434a-8e9c-9fe3abf5c3d52025-02-06WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661
DG Health Naproxen SodiumNAPROXEN SODIUMDolgencorp Inc534eaf8a-0d2a-4390-af92-af5c98ba56a52025-01-23WarningsExact identifier
application applno (ANDA): 074661
application number: ANDA074661

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
849574naproxen sodium 220 MG Oral TabletPSNe668c80f-dd53-4b82-8678-5e4fccb130236
849574naproxen sodium 220 MG Oral TabletSCDe668c80f-dd53-4b82-8678-5e4fccb130236
849574naproxen sodium 220 MG (as naproxen 200 MG) Oral TabletSYe668c80f-dd53-4b82-8678-5e4fccb130236

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63187-596-246318705962424 TABLET, FILM COATED in 1 BOTTLE (63187-596-24) 2017-09-010000-00-00NoNoCurrent
63187-596-286318705962828 TABLET, FILM COATED in 1 BOTTLE (63187-596-28) 2017-08-010000-00-00NoNoCurrent
63187-596-306318705963030 TABLET, FILM COATED in 1 BOTTLE (63187-596-30) 2015-08-030000-00-00NoNoCurrent
63187-596-606318705966090 TABLET, FILM COATED in 1 BOTTLE (63187-596-60) 2015-08-030000-00-00NoNoCurrent
63187-596-906318705969060 TABLET, FILM COATED in 1 BOTTLE (63187-596-90) 2015-08-030000-00-00NoNoCurrent