Home NDC 73057-376 Pharbetol
Product NDC 73057-376
11-digit product format 730570376
Labeler code 73057
Product ID 73057-376_2b899f07-4c46-cd87-e063-6294a90a4090
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen 500mg
Dosage form TABLET
Route ORAL
Labeler Ulai Health LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-08
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 3 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 73057-376 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 73057-376 73057-376-11 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 73057-376 73057-376-08 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 Pharbetol
Listing expiration 2026-12-31 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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198440 Internal RxNorm lookup 1293942 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73057-376-08 Pharbetol 100 in 1 BOTTLE, PLASTIC TABLET 100 3 73057-376-11 Pharbetol 1000 in 1 BOTTLE, PLASTIC TABLET 1000 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73057-376 PHARBETOL (ACETAMINOPHEN 500MG) TABLET [ULAI HEALTH LLC] 3 Current NDC, Legacy NDC, 2 package rows 20250114_e64ce7b1-4501-4b51-b012-1882ed153b42.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 39 of 79 · 1,579 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 73057-376-08 73057037608 100 TABLET in 1 BOTTLE, PLASTIC (73057-376-08) 100 tablet 2019-07-08 0000-00-00 No No Current 73057-376-11 73057037611 1000 TABLET in 1 BOTTLE, PLASTIC (73057-376-11) 1000 tablet 2019-07-08 0000-00-00 No No Current