Home NDC 58602-745 Acetaminophen Extra Strength
Product NDC 58602-745
11-digit product format 586020745
Labeler code 58602
Product ID 58602-745_0b44d6cf-d21e-741a-e063-6294a90a05ff
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler Aurohealth LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-07
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 Acetaminophen 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 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 58602-745-07 Acetaminophen Extra Strength 24 in 1 BOTTLE TABLET 24 2 58602-745-07 Acetaminophen Extra Strength 1 in 1 CARTON TABLET 1 2 58602-745-14 Acetaminophen Extra Strength 50 in 1 BOTTLE TABLET 50 2 58602-745-14 Acetaminophen Extra Strength 1 in 1 CARTON TABLET 1 2 58602-745-21 Acetaminophen Extra Strength 100 in 1 BOTTLE TABLET 100 2 58602-745-21 Acetaminophen Extra Strength 1 in 1 CARTON TABLET 1 2 58602-745-35 Acetaminophen Extra Strength 225 in 1 BOTTLE TABLET 225 2 58602-745-35 Acetaminophen Extra Strength 1 in 1 CARTON TABLET 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58602-745 ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [AUROHEALTH LLC] 2 Current NDC, Legacy NDC, 8 package rows 20231130_bc03fa56-8880-4bbd-81a0-91853fecdd4e.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 64 of 79 · 1,579 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 58602-745-07 58602074507 1 BOTTLE in 1 CARTON (58602-745-07) / 24 TABLET in 1 BOTTLE 1 bottle 2021-01-07 0000-00-00 No No Current 58602-745-14 58602074514 1 BOTTLE in 1 CARTON (58602-745-14) / 50 TABLET in 1 BOTTLE 1 bottle 2021-01-07 0000-00-00 No No Current 58602-745-21 58602074521 1 BOTTLE in 1 CARTON (58602-745-21) / 100 TABLET in 1 BOTTLE 1 bottle 2021-01-07 0000-00-00 No No Current 58602-745-35 58602074535 1 BOTTLE in 1 CARTON (58602-745-35) / 225 TABLET in 1 BOTTLE 1 bottle 2021-01-07 0000-00-00 No No Current