Home NDC 71205-456 ACETAMINOPHEN 325 MG
Product NDC 71205-456
11-digit product format 712050456
Labeler code 71205
Product ID 71205-456_d25dcece-12ac-4e85-a6ec-fd71d1dc1fde
Type HUMAN OTC DRUG
Nonproprietary name ACETAMINOPHEN
Dosage form TABLET
Route ORAL
Labeler Proficient Rx LP
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-11-01
Substance ACETAMINOPHEN
Active strength 325 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 325 MG
Listing expiration 2027-12-31 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 71205-456-00 ACETAMINOPHEN 325 MG 100 in 1 BOTTLE, PLASTIC TABLET 100 5 71205-456-30 ACETAMINOPHEN 325 MG 30 in 1 BOTTLE, PLASTIC TABLET 30 5 71205-456-60 ACETAMINOPHEN 325 MG 60 in 1 BOTTLE, PLASTIC TABLET 60 5 71205-456-90 ACETAMINOPHEN 325 MG 90 in 1 BOTTLE, PLASTIC TABLET 90 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71205-456 ACETAMINOPHEN 325 MG (ACETAMINOPHEN) TABLET [PROFICIENT RX LP] 4 Current NDC, Legacy NDC, 4 package rows 20240223_6794830a-7856-464d-84be-c8b253cf41ac.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 59 of 79 · 1,576 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 71205-456-00 71205045600 100 TABLET in 1 BOTTLE, PLASTIC (71205-456-00) 100 tablet 2020-06-15 0000-00-00 No No Current 71205-456-30 71205045630 30 TABLET in 1 BOTTLE, PLASTIC (71205-456-30) 30 tablet 2022-02-02 0000-00-00 No No Current 71205-456-60 71205045660 60 TABLET in 1 BOTTLE, PLASTIC (71205-456-60) 60 tablet 2022-02-02 0000-00-00 No No Current 71205-456-90 71205045690 90 TABLET in 1 BOTTLE, PLASTIC (71205-456-90) 90 tablet 2022-02-02 0000-00-00 No No Current