Home NDC 79903-032 EXTRA STRENGTH ACETAMINOPHEN
Product NDC 79903-032
11-digit product format 799030032
Labeler code 79903
Product ID 79903-032_495e1164-7604-42c2-e063-6394a90aa96d
Type HUMAN OTC DRUG
Nonproprietary name ACETAMINOPHEN
Dosage form TABLET
Route ORAL
Labeler Wal-Mart Stores Inc
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-05
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 EXTRA STRENGTH ACETAMINOPHEN
Listing expiration 2027-12-31 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 79903-032-01 EXTRA STRENGTH ACETAMINOPHEN 100 in 1 BOTTLE TABLET 100 9 79903-032-02 EXTRA STRENGTH ACETAMINOPHEN 2 in 1 CARTON TABLET 2 9 79903-032-10 EXTRA STRENGTH ACETAMINOPHEN 100 in 1 BOTTLE TABLET 100 9 79903-032-40 EXTRA STRENGTH ACETAMINOPHEN 1 in 1 CARTON TABLET 1 9 79903-032-40 EXTRA STRENGTH ACETAMINOPHEN 40 in 1 BOTTLE TABLET 40 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79903-032 EXTRA STRENGTH ACETAMINOPHEN (ACETAMINOPHEN) TABLET [WAL-MART STORES INC] 7 Current NDC, Legacy NDC, 5 package rows 20250101_a88eba4c-0701-4eec-9a24-a804186fbfd8.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 79903-032-01 79903003201 100 in 1 BOTTLE Historical 79903-032-02 79903003202 2 BOTTLE in 1 CARTON (79903-032-02) / 100 TABLET in 1 BOTTLE (79903-032-01) 2 bottle 2021-01-12 2028-09-30 No No Current 79903-032-10 79903003210 100 TABLET in 1 BOTTLE (79903-032-10) 100 tablet 2021-01-12 0000-00-00 No No Current 79903-032-40 79903003240 1 BOTTLE in 1 CARTON (79903-032-40) / 40 TABLET in 1 BOTTLE 1 bottle 2021-01-12 2029-04-30 No No Current