Home NDC 58602-754-07 Aurophen Regular Strength
Product NDC 58602-754
Requested package NDC 58602-754-07
11-digit product format 586020754
Labeler code 58602
Product ID 58602-754_0b463c9c-6ad9-20df-e063-6394a90a427a
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler Aurohealth LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-02-26
Substance ACETAMINOPHEN
Active strength 325 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 Regular Strength
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 325 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 313782 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 58602-754-07 Aurophen Regular Strength 24 in 1 BOTTLE TABLET 24 4 58602-754-07 Aurophen Regular Strength 1 in 1 CARTON TABLET 1 4 58602-754-14 Aurophen Regular Strength 50 in 1 BOTTLE TABLET 50 4 58602-754-14 Aurophen Regular Strength 1 in 1 CARTON TABLET 1 4 58602-754-21 Aurophen Regular Strength 100 in 1 BOTTLE TABLET 100 4 58602-754-21 Aurophen Regular Strength 1 in 1 CARTON TABLET 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58602-754 AUROPHEN REGULAR STRENGTH (ACETAMINOPHEN) TABLET [AUROHEALTH LLC] 4 Current NDC, Legacy NDC, 6 package rows 20231130_8eda893f-5266-4b7a-95b9-2e194973cf06.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 75 of 79 · 1,570 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 58602-754-07 58602075407 1 BOTTLE in 1 CARTON (58602-754-07) / 24 TABLET in 1 BOTTLE 1 bottle 2016-02-26 0000-00-00 No No Current