Home NDC 0363-0519-20 Pain Reliever
Product NDC 0363-0519
Requested package NDC 0363-0519-20
11-digit product format 003630519
Labeler code 0363
Product ID 0363-0519_47a1e1b6-6aea-4562-8c40-bcf5bfe79e4c
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, COATED
Route ORAL
Labeler Walgreen Company
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2004-05-10
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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…
Additional Listing Data#
Finished product Yes
Brand name base Pain Reliever
Brand name suffix Extra Strength
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198440 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0363-0519-08 Pain RelieverExtra Strength 1 in 1 CARTON TABLET, COATED 1 24 0363-0519-08 Pain RelieverExtra Strength 24 in 1 BOTTLE, PLASTIC TABLET, COATED 24 24 0363-0519-12 Pain RelieverExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET, COATED 100 24 0363-0519-12 Pain RelieverExtra Strength 1 in 1 CARTON TABLET, COATED 1 24 0363-0519-15 Pain RelieverExtra Strength 1 in 1 CARTON TABLET, COATED 1 24 0363-0519-15 Pain RelieverExtra Strength 50 in 1 BOTTLE, PLASTIC TABLET, COATED 50 24 0363-0519-19 Pain RelieverExtra Strength 8 in 1 VIAL TABLET, COATED 8 24 0363-0519-19 Pain RelieverExtra Strength 1 in 1 CARTON TABLET, COATED 1 24 0363-0519-20 Pain RelieverExtra Strength 225 in 1 BOTTLE, PLASTIC TABLET, COATED 225 24 0363-0519-20 Pain RelieverExtra Strength 1 in 1 CARTON TABLET, COATED 1 24 0363-0519-29 Pain RelieverExtra Strength 150 in 1 BOTTLE, PLASTIC TABLET, COATED 150 24 0363-0519-37 Pain RelieverExtra Strength 1 in 1 CARTON TABLET, COATED 1 24 0363-0519-37 Pain RelieverExtra Strength 75 in 1 BOTTLE, PLASTIC TABLET, COATED 75 24 0363-0519-54 Pain RelieverExtra Strength 375 in 1 BOTTLE, PLASTIC TABLET, COATED 375 24 0363-0519-92 Pain RelieverExtra Strength 150 in 1 BOTTLE, PLASTIC TABLET, COATED 150 24
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-0519 PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET, COATED [WALGREEN COMPANY] 23 Current NDC, Legacy NDC, 15 package rows 20250104_fa33f6ef-522b-4630-9716-92371d9cd24a.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 85 · 1,687 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0363-0519-20 00363051920 1 BOTTLE, PLASTIC in 1 CARTON (0363-0519-20) > 225 TABLET, COATED in 1 BOTTLE, PLASTIC 2004-05-10 0000-00-00 No No Current