Senna

Product NDC
71406-105
11-digit product format
714060105
Labeler code
71406
Product ID
71406-105_ebe1e1fd-ec42-e0f0-e053-2995a90a2467
Type
HUMAN OTC DRUG
Nonproprietary name
Sennosides 8.6 mg Tablets
Dosage form
TABLET
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
SENNOSIDES
Active strength
9 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71406-105DDiscontinued by firm2026-10-05
excluded packagepackage71406-10571406-105-01DDiscontinued by firm2026-10-05
excluded packagepackage71406-10571406-105-10DDiscontinued by firm2026-10-05

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 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage71406-105-01d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage71406-105-10d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage71406-105-01f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage71406-105-10f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71406-105-01EA - Each71406-1051c4ca8dd-59d6-498a-a0fb-024932d4ae2212021-11-09
71406-105-10EA - Each71406-10553afb42b-8473-41e5-9bea-2a02df8f9ae412021-11-09

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71406-105-0171406010501100 TABLET in 1 BOTTLE, PLASTIC (71406-105-01) 100 tablet2019-08-300000-00-00NoNoCurrent
71406-105-10714060105101000 TABLET in 1 BOTTLE, PLASTIC (71406-105-10) 1000 tablet2019-08-300000-00-00NoNoCurrent