basic care naproxen sodium pm

Product NDC
0113-7264
Requested package NDC
0113-7264-06
11-digit product format
001137264
Labeler code
0113
Product ID
0113-7264_6431fba1-429b-43ab-9ac1-3e8d1669bffd
Type
HUMAN OTC DRUG
Nonproprietary name
diphenhydramine hydrochloride, naproxen sodium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
L. Perrigo Company
Application
ANDA208499
Marketing category
ANDA
Marketing start
2020-01-09
Marketing end
0000-00-00
Substance
DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
Active strength
25 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
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 packagepackage0113-72640113-7264-06DDiscontinued 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
A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDEDIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM25MG;220MGTABLET / ORAL2019-05-10

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 UTC2026-02A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-1031067a03dcf5…
2025-08-23 18:47 UTC2025-08A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-106a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-1003ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-102680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-105bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-1079d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-101e350fbaab3a…
2024-05-31 18:47 UTC2024-05A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-108072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-105c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-105d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-104b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-1074a2ff9319b5…
2022-03-09 01:35 UTC2022-03A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-1087673890dc5c…
2021-03-12 10:30 UTC2021-03A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-105aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-108869cabd3fbd…
2020-11-12 02:37 UTC2020-11A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10c0c555d07b60…
2019-12-14 00:12 UTC2019-12A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-103f01610625f2…
2019-09-15 20:21 UTC2019-09A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10b00525d2431f…
2019-07-19 19:46 UTC2019-07A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-106a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-101c564ffb4f44…
2023-12-20 04:57 UTC2023-12A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-109b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-103f0d92c62455…
2023-05-13 08:27 UTC2023-05A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10053a50430f4f…
2023-01-26 05:58 UTC2023-01A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-103bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-103a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10f41ea6bd6efb…
2022-09-29 23:25 UTC2022-09A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10e64feba35796…
2022-07-09 03:26 UTC · 3 captures of this ZIP2022-07A208499-001NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE25MG;220MGTABLET / ORAL2019-05-10cb3db0bc1861…

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
naproxen sodium pmDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMMeijer Distribution Inc34d635f8-9703-4c29-92a5-85d3b47c4c932026-07-07WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
good sense naproxen sodiumDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUML. Perrigo Companyf548aa3d-b35e-458a-9815-3595a451ab782026-05-11WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
ALL NIGHT PAIN RELIEF PMDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMWalgreen Company43e4ed28-b1be-4548-86ac-f40f9f83f04e2026-04-27WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
naproxen sodium pmDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMH E B4281faf5-7182-404f-9f53-3d9ea0354a182026-02-12WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
topcare all night pain relief pmDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMTopco Associates LLCa20f193e-4e64-400a-b605-df08026cb80b2025-12-11WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
up and up naproxen sodium pmDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMTarget Corporationc0769941-bcf2-4237-b70c-a79089ad53352025-11-05WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
dg health naproxen sodium pmDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMDolgencorp Inc6c2c087c-e36d-4971-b977-d3cab6d6edee2025-11-05WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
naproxen sodium pmDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMKroger Companyd5dafdd0-968d-4ee6-9461-1f72d32552402025-07-10WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
NAPROXEN SODIUM PMDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMSafeway60cb7b6e-f2d2-48ca-8db7-7124717735d52025-07-09WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
equaline naproxen sodium pmDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMUnited Natural Foods, Inc. dba UNFIed7bfa3f-4972-4ab6-9f0c-0873a11571a92025-06-04WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
basic care naproxen sodium pmDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMAmazon.com Services LLC7beed9e7-816b-494b-93fa-9caf10aa38342024-01-24WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499
careone naproxen sodium pmDIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUMAmerican Sales Company16547905-59c0-4936-82e1-2d9f5935d8dd2023-12-11WarningsExact identifier
application applno (ANDA): 208499
application number: ANDA208499

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0113-7264-06001137264061 BOTTLE in 1 CARTON (0113-7264-06) > 160 TABLET, FILM COATED in 1 BOTTLE1 bottle2020-01-090000-00-00NoNoCurrent