Home NDC 55959-171-06 DOLO- NeuroBion
Product NDC 55959-171
Requested package NDC 55959-171-06
11-digit product format 559590171
Labeler code 55959
Product ID 55959-171_ecd800ee-edcd-42d8-9e95-f88210b41ee5
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler BENARD INDUSTRIES INC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-05-04
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Additional Listing Data#
Finished product Yes
Brand name base DOLO- NeuroBion
Brand name suffix Acetaminophen 500mg
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 · 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55959-171-03 DOLO- NeuroBionAcetaminophen 500mg 30 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 30 2 55959-171-03 DOLO- NeuroBionAcetaminophen 500mg 1 in 1 CARTON TABLET, FILM COATED 1 2 55959-171-06 DOLO- NeuroBionAcetaminophen 500mg 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 2 55959-171-06 DOLO- NeuroBionAcetaminophen 500mg 1 in 1 CARTON TABLET, FILM COATED 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55959-171 DOLO- NEUROBION ACETAMINOPHEN 500MG (ACETAMINOPHEN) TABLET, FILM COATED [BENARD INDUSTRIES INC] 2 Current NDC, Legacy NDC, 4 package rows 20241105_16f8415d-8190-4212-b487-c0caf7d3bee2.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 85 · 1,687 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 55959-171-06 55959017106 1 BOTTLE, PLASTIC in 1 CARTON (55959-171-06) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2016-05-04 0000-00-00 No No Current