Sennosides,Docusate sodium

Product NDC
0536-1169
11-digit product format
005361169
Labeler code
0536
Product ID
0536-1169_dae81e35-85a4-c319-e053-2995a90a113a
Type
HUMAN OTC DRUG
Nonproprietary name
Sennosides,Docusate sodium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Rugby Laboratories
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-12-13
Marketing end
2022-04-30
Substance
DOCUSATE SODIUM; SENNOSIDES
Active strength
50 mg/1; mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0536-1169-01EA - Each0536-1169f1e8649b-4385-4af2-9381-d9bed66b201b12019-02-13
0536-1169-10EA - Each0536-116954bc2640-c0b1-4c04-8c4a-b2e083b3871912019-01-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0536-1169-0100536116901100 TABLET, FILM COATED in 1 BOTTLE (0536-1169-01) 2018-12-130000-00-00NoNoCurrent
0536-1169-10005361169101000 TABLET, FILM COATED in 1 BOTTLE (0536-1169-10) 2018-12-170000-00-00NoNoCurrent