Flanax Pain Reliever/Fever Reducer

Product NDC
27854-700
11-digit product format
278540700
Labeler code
27854
Product ID
27854-700_4215c852-11ed-4b06-b132-3674265078e3
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen sodium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Belmora LLC
Application
ANDA205497
Marketing category
ANDA
Marketing start
2020-05-15
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

Source provenance: Browse the complete Orange Book source catalog · source snapshot 42.

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
A205497-001NAPROXEN SODIUMNAPROXEN SODIUM220MGTABLET / ORAL2016-03-18

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 · 42 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-08-18 06:07:402026-07A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1831067a03dcf5…
2025-08-23 18:47 UTC2025-08A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-186a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1803ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-182680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-185bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1879d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-181e350fbaab3a…
2024-05-31 18:47 UTC2024-05A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-188072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-185c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-185d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-184b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1874a2ff9319b5…
2022-03-09 01:35 UTC2022-03A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1887673890dc5c…
2021-03-12 10:30 UTC2021-03A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-185aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-188869cabd3fbd…
2020-11-12 02:37 UTC2020-11A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18c0c555d07b60…
2019-12-14 00:12 UTC2019-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-183f01610625f2…
2019-09-15 20:21 UTC2019-09A205497-001NAPROXEN SODIUMEQ 200MG BASETABLET / ORAL2016-03-18b00525d2431f…
2019-07-19 19:46 UTC2019-07A205497-001NAPROXEN SODIUMEQ 200MG BASETABLET / ORAL2016-03-18ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-186a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-181c564ffb4f44…
2023-12-20 04:57 UTC2023-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-189b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-183f0d92c62455…
2023-05-13 08:27 UTC2023-05A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18053a50430f4f…
2023-01-26 05:58 UTC2023-01A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-183bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-183a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18f41ea6bd6efb…
2022-09-29 23:25 UTC2022-09A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18e64feba35796…

Additional Listing Data#

Finished product
Yes
Brand name base
Flanax Pain Reliever/Fever Reducer
Listing expiration
2026-12-31

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
a93e4966-9dd3-40ba-b7d6-6ca8fef229c6Available 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
27854-700-01Flanax Pain Reliever/Fever Reducer24 in 1 BOTTLETABLET, FILM COATED241
27854-700-01Flanax Pain Reliever/Fever Reducer1 in 1 CARTONTABLET, FILM COATED11
27854-700-10Flanax Pain Reliever/Fever Reducer10 in 1 BOTTLETABLET, FILM COATED101
27854-700-10Flanax Pain Reliever/Fever Reducer1 in 1 CARTONTABLET, FILM COATED11
27854-700-99Flanax Pain Reliever/Fever Reducer1 in 1 CARTONTABLET, FILM COATED11
27854-700-99Flanax Pain Reliever/Fever Reducer100 in 1 BOTTLETABLET, FILM COATED1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
27854-700FLANAX PAIN RELIEVER/FEVER REDUCER (NAPROXEN SODIUM) TABLET, FILM COATED [BELMORA LLC]1Current NDC, Legacy NDC, 6 package rows20200523_a93e4966-9dd3-40ba-b7d6-6ca8fef229c6.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 1 of 1 · 12 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AMAZON BASIC CARE NAPROXEN SODIUMNAPROXEN SODIUMAmazon.com Services LLC10ee5bc0-509d-b549-e063-6394a90a5dca2025-05-26WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Naproxen Sodium HEADACHE PAINNAPROXEN SODIUMAurohealth LLC10464576-0f9a-4a64-a388-3afe336829382025-05-26WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Naproxen SodiumNAPROXEN SODIUMAurohealth LLC2dfa820c-5130-43b0-9e63-19354bbbd3c32025-05-26WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Naproxen Sodium BACK AND MUSCLE PAINNAPROXEN SODIUMAurohealth LLC666e3c6a-e571-4124-84d8-0142db1012dc2025-05-26WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Naproxen SodiumNAPROXEN SODIUMAurohealth LLCd570f8f3-88b8-408d-8d20-3ca5f64c81f82025-05-23WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Naproxen SodiumNAPROXEN SODIUMAurohealth LLC46a15412-25d6-454d-86db-70321d19a2c92025-05-23WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Naproxen SodiumNAPROXEN SODIUMWALMART INC.1292c0ca-343e-adcc-e063-6394a90ab9fa2025-05-23WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Naproxen Sodium HEADACHE PAINNAPROXEN SODIUMAurohealth LLCe4a9ea0e-aec4-493c-b9b4-5e5a91d260d52025-05-23WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Naproxen Sodium BACK AND MUSCLE PAINNAPROXEN SODIUMAurohealth LLCc2066fce-cfa2-426d-ab6d-1a426736612b2025-05-23WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Naproxen SodiumNAPROXEN SODIUMWALMART INC.09b52dd4-0434-237c-e063-6294a90ab9b52025-05-23WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Ana-Dent PAIN RELIEFNAPROXEN SODIUMBelmora LLC04721306-2850-4e0a-9dd9-7cabb575f3c72020-05-18WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
Flanax Pain Reliever/Fever ReducerNAPROXEN SODIUMBelmora LLCa93e4966-9dd3-40ba-b7d6-6ca8fef229c62020-05-15WarningsExact identifier
application applno (ANDA): 205497
application number: ANDA205497
ndc (product): 27854-700

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
849574naproxen sodium 220 MG Oral TabletPSNa93e4966-9dd3-40ba-b7d6-6ca8fef229c61
849574naproxen sodium 220 MG Oral TabletSCDa93e4966-9dd3-40ba-b7d6-6ca8fef229c61
849574naproxen sodium 220 MG (as naproxen 200 MG) Oral TabletSYa93e4966-9dd3-40ba-b7d6-6ca8fef229c61

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
27854-700-01278540700011 BOTTLE in 1 CARTON (27854-700-01) / 24 TABLET, FILM COATED in 1 BOTTLE1 bottle2020-05-150000-00-00NoNoCurrent
27854-700-10278540700101 BOTTLE in 1 CARTON (27854-700-10) / 10 TABLET, FILM COATED in 1 BOTTLE1 bottle2020-05-150000-00-00NoNoCurrent
27854-700-99278540700991 BOTTLE in 1 CARTON (27854-700-99) / 100 TABLET, FILM COATED in 1 BOTTLE1 bottle2020-05-150000-00-00NoNoCurrent