Home NDC 50844-175-94 Pain Reliever
Product NDC 50844-175
Requested package NDC 50844-175-94
11-digit product format 508440175
Labeler code 50844
Product ID 50844-175_195fd310-b148-478a-aad5-2894a0ace24c
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler L.N.K. International, Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 1993-04-02
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 Pain Reliever
Brand name suffix Extra Strength
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 50844-175-08 Pain RelieverExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 14 50844-175-08 Pain RelieverExtra Strength 24 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 24 14 50844-175-10 Pain RelieverExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 14 50844-175-10 Pain RelieverExtra Strength 40 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 40 14 50844-175-12 Pain RelieverExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 14 50844-175-12 Pain RelieverExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 14 50844-175-94 Pain RelieverExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 14
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50844-175 PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 14 Current NDC, Legacy NDC, 7 package rows 20250116_8fed703a-9de2-4c76-a783-fcf004f9b890.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 33 of 79 · 1,561 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 50844-175-94 50844017594 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-175-94) 1993-04-02 0000-00-00 No No Current