Home NDC 76420-488-12 ACETAMINOPHEN 500 MG
Product NDC 76420-488
Requested package NDC 76420-488-12
11-digit product format 764200488
Labeler code 76420
Product ID 76420-488_5fe87e72-2b97-6922-e063-6394a90a9182
Type HUMAN OTC DRUG
Nonproprietary name ACETAMINOPHEN
Dosage form TABLET
Route ORAL
Labeler ASCLEMED USA INC.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-11-01
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
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 500 MG
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76420-488-01 ACETAMINOPHEN 500 MG 100 in 1 BOTTLE, PLASTIC TABLET 100 1 76420-488-10 ACETAMINOPHEN 500 MG 10 in 1 BOTTLE, PLASTIC TABLET 10 1 76420-488-20 ACETAMINOPHEN 500 MG 20 in 1 BOTTLE, PLASTIC TABLET 20 1 76420-488-30 ACETAMINOPHEN 500 MG 30 in 1 BOTTLE, PLASTIC TABLET 30 1 76420-488-60 ACETAMINOPHEN 500 MG 60 in 1 BOTTLE, PLASTIC TABLET 60 1 76420-488-90 ACETAMINOPHEN 500 MG 90 in 1 BOTTLE, PLASTIC TABLET 90 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 77 · 1,530 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 76420-488-12 76420048812 120 TABLET in 1 BOTTLE, PLASTIC (76420-488-12) 120 tablet 2026-11-10 No No Current