Home NDC 0121-1882 Acetaminophen
Product NDC 0121-1882
11-digit product format 001211882
Labeler code 0121
Product ID 0121-1882_bbd6f65a-a6ec-4c17-935c-ed743c45e2c8
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form SUSPENSION
Route ORAL
Labeler PAI Holdings, LLC dba PAI Pharma
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-09-03
Substance ACETAMINOPHEN
Active strength 325 mg/10.15mL
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 · 2 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0121-1882 0121-1882-94 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0121-1882 0121-1882-94 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Additional Listing Data#
Finished product Yes
Brand name base Acetaminophen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 325 mg/10.15mL
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 307668 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0121-1882-00 Acetaminophen 10 in 1 CASE SUSPENSION 10 5 0121-1882-00 Acetaminophen 10 in 1 TRAY SUSPENSION 10 5 0121-1882-11 Acetaminophen 10.15 mL in 1 CUP, UNIT-DOSE SUSPENSION 10.15 5 0121-1882-94 Acetaminophen 3 in 1 CASE SUSPENSION 3 5 0121-1882-94 Acetaminophen 10 in 1 TRAY SUSPENSION 10 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0121-1882 ACETAMINOPHEN SUSPENSION [PAI HOLDINGS, LLC DBA PAI PHARMA] 4 Current NDC, Legacy NDC, 5 package rows 20241114_caf5daea-409e-5dd2-e053-2995a90acb12.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 Units Marketing start Marketing end Sample Exclude flag Status 0121-1882-00 00121188200 10 TRAY in 1 CASE (0121-1882-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10.15 mL in 1 CUP, UNIT-DOSE (0121-1882-11) 10 tray 2021-09-03 0000-00-00 No No Current 0121-1882-11 00121188211 10.15 mL in 1 CUP, UNIT-DOSE 10.15 ml Historical 0121-1882-94 00121188294 3 TRAY in 1 CASE (0121-1882-94) > 10 CUP, UNIT-DOSE in 1 TRAY > 10.15 mL in 1 CUP, UNIT-DOSE (0121-1882-11) 3 tray 2021-09-03 0000-00-00 No No Current