Naproxen Sodium

Product NDC
30142-748
Requested package NDC
30142-748-16
11-digit product format
301420748
Labeler code
30142
Product ID
30142-748_e02ba5d6-1d30-4bea-abd8-1327807e280c
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen Sodium
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
The Kroger Co.
Application
ANDA208363
Marketing category
ANDA
Marketing start
2018-04-01
Marketing end
2024-05-31
Substance
NAPROXEN SODIUM
Active strength
220 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage30142-74830142-748-16DDiscontinued by firm2026-08-03

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

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
A208363-001NAPROXEN SODIUMNAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15

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 · 41 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-02-19 14:30 UTC2026-02A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-1531067a03dcf5…
2025-08-23 18:47 UTC2025-08A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-156a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-1503ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-152680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-155bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-1579d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-151e350fbaab3a…
2024-05-31 18:47 UTC2024-05A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-158072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-155c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-155d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-154b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-1574a2ff9319b5…
2022-03-09 01:35 UTC2022-03A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-1587673890dc5c…
2021-03-12 10:30 UTC2021-03A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-155aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-158869cabd3fbd…
2020-11-12 02:37 UTC2020-11A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15c0c555d07b60…
2019-12-14 00:12 UTC2019-12A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-153f01610625f2…
2019-09-15 20:21 UTC2019-09A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15b00525d2431f…
2019-07-19 19:46 UTC2019-07A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-156a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-151c564ffb4f44…
2023-12-20 04:57 UTC2023-12A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-159b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-153f0d92c62455…
2023-05-13 08:27 UTC2023-05A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15053a50430f4f…
2023-01-26 05:58 UTC2023-01A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-153bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-153a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15f41ea6bd6efb…
2022-09-29 23:25 UTC2022-09A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15e64feba35796…
2022-07-09 03:26 UTC · 3 captures of this ZIP2022-07A208363-001NAPROXEN SODIUMEQ 200MG BASECAPSULE / ORAL2018-03-15cb3db0bc1861…

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 · 17 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Naproxen SodiumNAPROXEN SODIUMEQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)c28c4fd2-1428-421c-b62f-265e472d833e2026-07-09WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMCVS Pharmacyc194124b-a5f6-423e-bc9a-7b611df990a82026-05-13WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMWalgreensd9806ad8-1cea-4599-97ef-a956ec7f0e212026-03-11WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMSafeway, Inc.deb1be0f-64ae-46b5-b54a-1a58eec6492e2026-01-05WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMP & L Development, LLCfc65fe79-c93b-4247-b9af-e562792a3e642025-08-19WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMAAFES/Your Military Exchangesc387f7cb-7cc4-4989-9f9a-bb00a895fd0d2025-05-08WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMProductos Zapotol Corp.6386f6f6-9bc7-4b85-ac87-03fd147259042024-03-14WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMProductos Zapotol Corp.0a69f39e-5eb6-4a98-85f0-87e7449672d62024-03-14WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMCare One (Retail Business Services, LLC.)5582d6e1-4937-43f6-a92c-9d5f9ef1a3ad2024-02-21WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
All Day ReliefNAPROXEN SODIUMPublix Supermarkets, Inc.4db86c5b-62bb-4638-9f1e-98dc2680d6cc2024-01-23WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMTARGET Corporation36ce5cd9-8c61-4ed9-b840-c29ad98bdfc52023-10-25WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMStrategic Sourcing Services LLC435e55b2-3d75-4a1e-9f00-69b29baf37af2023-10-02WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMCare One (American Sales Company)043f7032-4e83-4642-93a8-6c09de26b43f2022-11-21WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMStrategic Sourcing Services LLCa636037d-127c-478d-9d61-dda6eafd2e812022-11-15WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
Naproxen SodiumNAPROXEN SODIUMDolgencorp, Inc. (DOLLAR GENERAL & REXALL)de03311d-fb58-43f5-a110-aac9a39c91322022-11-07WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
NAPROXEN SODIUMNAPROXEN SODIUMPuraCap Pharmaceutical LLCfc865e81-164c-48e9-8fb9-6fc27d1c33cf2019-12-10WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363
NAPROXEN SODIUMNAPROXEN SODIUMHumanwell PuraCap Pharmaceuticals (Wuhan) Co., Ltd1d5981dd-e3f5-48a3-a5f1-ce49689cdfac2019-11-08WarningsExact identifier
application applno (ANDA): 208363
application number: ANDA208363

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-748-16301420748161 BOTTLE in 1 BOX (30142-748-16) > 160 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2018-04-012024-05-31NoNoCurrent