Home NDC 63940-174 All Day Pain Relief
Product NDC 63940-174
11-digit product format 639400174
Labeler code 63940
Product ID 63940-174_09662619-9516-4024-91bc-e877eef7dc97
Type HUMAN OTC DRUG
Nonproprietary name Naproxen Sodium
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler Harmon Stores
Application NDA021920
Marketing category NDA
Marketing start 2015-07-31
Marketing end 2020-12-31
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 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 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 63940-174-40 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 63940-174-40 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 63940-174-40 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 63940-174-40 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 63940-174-40 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 63940-174-40 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 63940-174-40 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 63940-174-40 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 63940-174-40 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 63940-174-40 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 63940-174-40 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 63940-174-40 557ba5c1ecfa…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-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N021920-001 NAPROXEN SODIUM NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17
Orange Book patents# Current patent rows page 1 of 1 · 8 matching rows.
Application-product, Patent, Expiration table Application-product Patent Expiration Use code Coverage / status Submission date N021920-001 10022344 2026-03-03 U-1731 Drug product 2018-07-23 N021920-001 10022344 2026-03-03 U-1732 Drug product 2018-07-23 N021920-001 10028925 2026-03-03 U-1731 Drug product 2018-07-24 N021920-001 10028925 2026-03-03 U-1732 Drug product 2018-07-24 N021920-001 11090280 2026-03-03 U-1731 Drug product 2021-08-24 N021920-001 11090280 2026-03-03 U-1732 Drug product 2021-08-24 N021920-001 9693978 2026-03-03 Drug product 2017-11-13 N021920-001 9693979 2026-03-03 Drug product 2017-11-13
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 · 41 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 2026-02-19 14:30 UTC 2026-02 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 782e0a99824c…2021-05-05 16:15 UTC · 3 captures of this ZIP 2021-05 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 87673890dc5c…2021-03-12 10:30 UTC 2021-03 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 5aa47cf7b7d7…2020-12-22 03:56 UTC 2020-12 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 8869cabd3fbd…2020-11-12 02:37 UTC 2020-11 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 c0c555d07b60…2019-12-14 00:12 UTC 2019-12 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 3f01610625f2…2019-09-15 20:21 UTC 2019-09 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 b00525d2431f…2019-07-19 19:46 UTC 2019-07 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 ea99ee380514…2024-03-16 18:09 UTC · 4 captures of this ZIP 2024-03 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 6a51e52b5d6a…2024-02-18 07:12 UTC 2024-02 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 1c564ffb4f44…2023-12-20 04:57 UTC 2023-12 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 ea1830bbd6c7…2023-11-28 05:40 UTC · 2 captures of this ZIP 2023-11 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 a72a2bbeb626…2023-10-25 00:34 UTC · 2 captures of this ZIP 2023-10 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 9b2671bbb829…2023-07-15 15:27 UTC · 2 captures of this ZIP 2023-07 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 a67488948f0b…2023-06-13 01:57 UTC · 3 captures of this ZIP 2023-06 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 3f0d92c62455…2023-05-13 08:27 UTC 2023-05 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 053a50430f4f…2023-01-26 05:58 UTC 2023-01 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 3bdfa0b2c4d7…2022-11-12 20:34 UTC · 5 captures of this ZIP 2022-11 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 3a93d1ddd44b…2022-10-28 04:53 UTC 2022-10 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 N021920-001 NAPROXEN SODIUM EQ 200MG BASE CAPSULE / ORAL RLD, RS 2006-02-17 cb3db0bc1861…
Observed Orange Book patent history# Patent history page 1 of 8 · 313 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Patent Expiration Use code Coverage / status Submission date Source SHA-256 2026-02-19 14:30 UTC 2026-02 N021920-001 10022344 2026-03-03 U-1731 Drug product 2018-07-23 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021920-001 10022344 2026-03-03 U-1732 Drug product 2018-07-23 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021920-001 10028925 2026-03-03 U-1731 Drug product 2018-07-24 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021920-001 10028925 2026-03-03 U-1732 Drug product 2018-07-24 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021920-001 11090280 2026-03-03 U-1731 Drug product 2021-08-24 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021920-001 11090280 2026-03-03 U-1732 Drug product 2021-08-24 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021920-001 9693978 2026-03-03 Drug product 2017-11-13 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N021920-001 9693979 2026-03-03 Drug product 2017-11-13 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N021920-001 10022344 2026-03-03 U-1731 Drug product 2018-07-23 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N021920-001 10022344 2026-03-03 U-1732 Drug product 2018-07-23 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N021920-001 10028925 2026-03-03 U-1731 Drug product 2018-07-24 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N021920-001 10028925 2026-03-03 U-1732 Drug product 2018-07-24 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N021920-001 11090280 2026-03-03 U-1731 Drug product 2021-08-24 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N021920-001 11090280 2026-03-03 U-1732 Drug product 2021-08-24 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N021920-001 9693978 2026-03-03 Drug product 2017-11-13 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N021920-001 9693979 2026-03-03 Drug product 2017-11-13 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N021920-001 10022344 2026-03-03 U-1731 Drug product 2018-07-23 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N021920-001 10022344 2026-03-03 U-1732 Drug product 2018-07-23 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N021920-001 10028925 2026-03-03 U-1731 Drug product 2018-07-24 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N021920-001 10028925 2026-03-03 U-1732 Drug product 2018-07-24 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N021920-001 11090280 2026-03-03 U-1731 Drug product 2021-08-24 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N021920-001 11090280 2026-03-03 U-1732 Drug product 2021-08-24 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N021920-001 9693978 2026-03-03 Drug product 2017-11-13 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N021920-001 9693979 2026-03-03 Drug product 2017-11-13 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N021920-001 10022344 2026-03-03 U-1731 Drug product 2018-07-23 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N021920-001 10022344 2026-03-03 U-1732 Drug product 2018-07-23 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N021920-001 10028925 2026-03-03 U-1731 Drug product 2018-07-24 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N021920-001 10028925 2026-03-03 U-1732 Drug product 2018-07-24 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N021920-001 11090280 2026-03-03 U-1731 Drug product 2021-08-24 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N021920-001 11090280 2026-03-03 U-1732 Drug product 2021-08-24 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N021920-001 9693978 2026-03-03 Drug product 2017-11-13 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N021920-001 9693979 2026-03-03 Drug product 2017-11-13 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N021920-001 10022344 2026-03-03 U-1731 Drug product 2018-07-23 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N021920-001 10022344 2026-03-03 U-1732 Drug product 2018-07-23 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N021920-001 10028925 2026-03-03 U-1731 Drug product 2018-07-24 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N021920-001 10028925 2026-03-03 U-1732 Drug product 2018-07-24 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N021920-001 11090280 2026-03-03 U-1731 Drug product 2021-08-24 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N021920-001 11090280 2026-03-03 U-1732 Drug product 2021-08-24 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N021920-001 9693978 2026-03-03 Drug product 2017-11-13 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N021920-001 9693979 2026-03-03 Drug product 2017-11-13 b8a1b40f171c…
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded NAPROXEN SODIUM ACTIVE INGREDIENT 9TN87S3A3C ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 NAPROXEN ACTIVE MOIETY 57Y76R9ATQ ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 GELATIN INACTIVE INGREDIENT 2G86QN327L ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 LACTIC ACID, UNSPECIFIED FORM INACTIVE INGREDIENT 33X04XA5AT ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 MANNITOL INACTIVE INGREDIENT 3OWL53L36A ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 POLYETHYLENE GLYCOL 600 INACTIVE INGREDIENT NL4J9F21N9 ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 POVIDONE K30 INACTIVE INGREDIENT U725QWY32X ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 SORBITAN INACTIVE INGREDIENT 6O92ICV9RU ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ALL DAY PAIN RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [HARMON STORES] 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 2 · 22 matching rows.