Home NDC 17714-133-50 ACETAMINOPHEN PM
Product NDC 17714-133
Requested package NDC 17714-133-50
11-digit product format 177140133
Labeler code 17714
Product ID 17714-133_60f41580-e074-faad-e053-2a91aa0a9076
Type HUMAN OTC DRUG
Nonproprietary name ACETAMINOPHEN PM
Dosage form TABLET
Route ORAL
Labeler Advance Pharmaceutical Inc.
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 2002-01-09
Substance ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength 500; 25 mg/1; mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base ACETAMINOPHEN PM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1 DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup TC2D6JAD40 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1092189 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 17714-133-50 ACETAMINOPHEN PM 50 in 1 BOTTLE TABLET 50 2
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17714-133 ACETAMINOPHEN PM TABLET [ADVANCE PHARMACEUTICAL INC.] 2 Current NDC, Legacy NDC, 1 package rows 20171223_b172226e-8f2a-4d9c-b7c7-dd737b90463a.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 1 · 1 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 17714-133-50 17714013350 50 TABLET in 1 BOTTLE (17714-133-50) 50 tablet 2002-01-09 0000-00-00 No No Current