Home NDC 58602-771 Aurophen Extra Strength for Adults
Product NDC 58602-771
11-digit product format 586020771
Labeler code 58602
Product ID 58602-771_0b45ad4e-d9d9-d463-e063-6294a90a195d
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler Aurohealth LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-08-21
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Aurophen Extra Strength for Adults
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 58602-771-36 Aurophen Extra Strength for Adults 250 in 1 BOTTLE TABLET 250 3 58602-771-40 Aurophen Extra Strength for Adults 500 in 1 BOTTLE TABLET 500 3 58602-771-41 Aurophen Extra Strength for Adults 1000 in 1 BOTTLE TABLET 1000 3 58602-771-64 Aurophen Extra Strength for Adults 600 in 1 BOTTLE TABLET 600 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58602-771 AUROPHEN EXTRA STRENGTH FOR ADULTS (ACETAMINOPHEN) TABLET [AUROHEALTH LLC] 3 Current NDC, Legacy NDC, 4 package rows 20231130_d59c5f04-4bcc-4a52-a42f-e049506f00de.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 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 58602-771-36 58602077136 250 TABLET in 1 BOTTLE (58602-771-36) 250 tablet 2020-08-21 0000-00-00 No No Current 58602-771-40 58602077140 500 TABLET in 1 BOTTLE (58602-771-40) 500 tablet 2020-08-21 0000-00-00 No No Current 58602-771-41 58602077141 1000 TABLET in 1 BOTTLE (58602-771-41) 1000 tablet 2020-08-21 0000-00-00 No No Current 58602-771-64 58602077164 600 TABLET in 1 BOTTLE (58602-771-64) 600 tablet 2021-05-17 0000-00-00 No No Current