Home NDC 87339-001-00 Parry-500mg Acetaminophen
Product NDC 87339-001
Requested package NDC 87339-001-00
11-digit product format 873390001
Labeler code 87339
Product ID 87339-001_4fac33dd-e6dc-879e-e063-6294a90a99f8
Type HUMAN OTC DRUG
Nonproprietary name ACETAMINOPHEN
Dosage form TABLET
Route ORAL
Labeler MDC PHARMACEUTICALS LIMITED
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-01
Substance ACETAMINOPHEN
Active strength 500 mg/1
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Parry-500mg 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.
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 84 · 1,678 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Status 87339-001-00 87339000100 50 TABLET in 1 BOTTLE, PLASTIC (87339-001-00) 50 tablet 2026-06-01 0 Current