Home NDC 71406-106-01 Senna-S
Product NDC 71406-106
Requested package NDC 71406-106-01
11-digit product format 714060106
Labeler code 71406
Product ID 71406-106_eb8f0eab-a05c-c489-e053-2995a90a4f17
Type HUMAN OTC DRUG
Nonproprietary name Docusate Sodium 50 mg Sennosides 8.6 mg
Dosage form TABLET, FILM COATED
Route ORAL
Labeler AACE PHARMACEUTICALS, INC.
Application part334
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2019-08-30
Marketing end 0000-00-00
Substance DOCUSATE SODIUM; SENNOSIDES
Active strength 50 mg/1; mg/1
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record 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 71406-106 71406-106-01 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 71406-106 71406-106-01 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 71406-106-01 71406010601 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71406-106-01) 2019-08-30 0000-00-00 No No Current