Senna-S

Product NDC
71406-106
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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71406-106-01EA - Each71406-106f9c40606-8818-4f2b-860d-2c879d9100d512021-11-09
71406-106-10EA - Each71406-10648c2bece-df8f-4c88-ad77-57a69f41f09d12021-11-09

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71406-106-0171406010601100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71406-106-01) 2019-08-300000-00-00NoNoCurrent
71406-106-10714060106101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71406-106-10) 2019-08-300000-00-00NoNoCurrent