Home NDC 49035-255-30 Naproxen Sodium
Product NDC 49035-255
Requested package NDC 49035-255-30
11-digit product format 490350255
Labeler code 49035
Product ID 49035-255_e460fb4c-b2cf-43a9-9726-e9fc952b637b
Type HUMAN OTC DRUG
Nonproprietary name Naproxen Sodium
Dosage form TABLET
Route ORAL
Labeler EQUATE (Wal-Mart Stores, Inc.)
Application ANDA091353
Marketing category ANDA
Marketing start 2014-04-30
Marketing end 2021-04-30
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 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 date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A091353-001 NAPROXEN SODIUM NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20
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 Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-18 06:07:40 2026-07 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 782e0a99824c…2021-05-05 16:15 UTC · 3 captures of this ZIP 2021-05 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 87673890dc5c…2021-03-12 10:30 UTC 2021-03 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 5aa47cf7b7d7…2020-12-22 03:56 UTC 2020-12 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 8869cabd3fbd…2020-11-12 02:37 UTC 2020-11 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 c0c555d07b60…2019-12-14 00:12 UTC 2019-12 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 3f01610625f2…2019-09-15 20:21 UTC 2019-09 A091353-001 NAPROXEN SODIUM EQ 200MG BASE TABLET / ORAL 2011-09-20 b00525d2431f…2019-07-19 19:46 UTC 2019-07 A091353-001 NAPROXEN SODIUM EQ 200MG BASE TABLET / ORAL 2011-09-20 ea99ee380514…2024-03-16 18:09 UTC · 4 captures of this ZIP 2024-03 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 6a51e52b5d6a…2024-02-18 07:12 UTC 2024-02 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 1c564ffb4f44…2023-12-20 04:57 UTC 2023-12 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 ea1830bbd6c7…2023-11-28 05:40 UTC · 2 captures of this ZIP 2023-11 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 a72a2bbeb626…2023-10-25 00:34 UTC · 2 captures of this ZIP 2023-10 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 9b2671bbb829…2023-07-15 15:27 UTC · 2 captures of this ZIP 2023-07 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 a67488948f0b…2023-06-13 01:57 UTC · 3 captures of this ZIP 2023-06 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 3f0d92c62455…2023-05-13 08:27 UTC 2023-05 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 053a50430f4f…2023-01-26 05:58 UTC 2023-01 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 3bdfa0b2c4d7…2022-11-12 20:34 UTC · 5 captures of this ZIP 2022-11 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 3a93d1ddd44b…2022-10-28 04:53 UTC 2022-10 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 A091353-001 NAPROXEN SODIUM 220MG TABLET / ORAL 2011-09-20 e64feba35796…
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded NAPROXEN SODIUM ACTIVE INGREDIENT 9TN87S3A3C NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 NAPROXEN ACTIVE MOIETY 57Y76R9ATQ NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 ALUMINUM OXIDE INACTIVE INGREDIENT LMI26O6933 NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 FD&C BLUE NO. 2 INACTIVE INGREDIENT L06K8R7DQK NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 POVIDONE K30 INACTIVE INGREDIENT U725QWY32X NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 SODIUM STARCH GLYCOLATE TYPE A CORN INACTIVE INGREDIENT AG9B65PV6B NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP NAPROXEN SODIUM TABLET [EQUATE (WALMART STORES, INC.)] 1
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 · 14 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49035-255-30 49035025530 300 TABLET in 1 BOTTLE, PLASTIC (49035-255-30) 300 tablet 2014-04-30 2021-04-30 No No Current