Home NDC 17714-124-10 SENNA-S
Product NDC 17714-124
Requested package NDC 17714-124-10
11-digit product format 177140124
Labeler code 17714
Product ID 17714-124_5cc973b8-e563-2f6c-e053-2a91aa0a9ab8
Type HUMAN OTC DRUG
Nonproprietary name Senna and Docusate Sodium Tablets, 8.6 mg and 50 mg
Dosage form TABLET
Route ORAL
Labeler Advance Pharmaceutical Inc.
Application part334
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2017-02-01
Marketing end 0000-00-00
Substance SENNOSIDES; DOCUSATE SODIUM
Active strength 9 mg/1; mg/1
NDC exclude flag No
Listing certified through 2020-12-31
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 · 15 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…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 17714-124-10 SENNA-S 1000 in 1 BOTTLE TABLET 1000 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17714-124 SENNA-S (SENNA AND DOCUSATE SODIUM TABLETS, 8.6 MG AND 50 MG) TABLET [ADVANCE PHARMACEUTICAL INC.] 2 Legacy NDC, 1 package rows 20171031_eccac127-5175-4a2e-828d-c9dd87713bb8.zip
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 17714-124-10 17714012410 1000 TABLET in 1 BOTTLE (17714-124-10) 1000 tablet 2017-02-01 0000-00-00 No No Current