Home NDC 71205-478 Pharbetol
Product NDC 71205-478
11-digit product format 712050478
Labeler code 71205
Product ID 71205-478_27ee285e-c641-4364-bd4a-7273b8e0cad2
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 2006-01-10
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 Pharbetol
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 · 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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71205-478-20 Pharbetol 20 in 1 BOTTLE, PLASTIC TABLET 20 5 71205-478-24 Pharbetol 24 in 1 BOTTLE, PLASTIC TABLET 24 5 71205-478-30 Pharbetol 30 in 1 BOTTLE, PLASTIC TABLET 30 5 71205-478-40 Pharbetol 40 in 1 BOTTLE, PLASTIC TABLET 40 5 71205-478-50 Pharbetol 50 in 1 BOTTLE, PLASTIC TABLET 50 5 71205-478-60 Pharbetol 60 in 1 BOTTLE, PLASTIC TABLET 60 5 71205-478-90 Pharbetol 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 71205-478 PHARBETOL (ACETAMINOPHEN) TABLET [PROFICIENT RX LP] 5 Current NDC, Legacy NDC, 7 package rows 20240131_51ba690e-d76b-41c6-a083-8bc803e1faa2.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 83 · 1,657 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 71205-478-20 71205047820 20 TABLET in 1 BOTTLE, PLASTIC (71205-478-20) 20 tablet 2024-01-26 No No Current 71205-478-24 71205047824 24 TABLET in 1 BOTTLE, PLASTIC (71205-478-24) 24 tablet 2020-09-30 0000-00-00 No No Current 71205-478-30 71205047830 30 TABLET in 1 BOTTLE, PLASTIC (71205-478-30) 30 tablet 2020-09-30 0000-00-00 No No Current 71205-478-40 71205047840 40 TABLET in 1 BOTTLE, PLASTIC (71205-478-40) 40 tablet 2020-10-12 0000-00-00 No No Current 71205-478-50 71205047850 50 TABLET in 1 BOTTLE, PLASTIC (71205-478-50) 50 tablet 2020-10-12 0000-00-00 No No Current 71205-478-60 71205047860 60 TABLET in 1 BOTTLE, PLASTIC (71205-478-60) 60 tablet 2020-09-30 0000-00-00 No No Current 71205-478-90 71205047890 90 TABLET in 1 BOTTLE, PLASTIC (71205-478-90) 90 tablet 2020-09-30 0000-00-00 No No Current