gentle laxative

Product NDC
49348-032
11-digit product format
493480032
Labeler code
49348
Product ID
49348-032_cdbd6e9c-63c7-421a-91c0-cf8450d91c45
Type
HUMAN OTC DRUG
Nonproprietary name
Bisacodyl
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Strategic Sourcing Services, LLC (Sunmark)
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2002-03-25
Marketing end
0000-00-00
Substance
BISACODYL
Active strength
5 mg/1
Pharmacologic classes
Increased Large Intestinal Motility [PE], Stimulant Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49348-032-05EA - Each49348-0324e529213-9481-4bee-be5b-d201bae6c8df12016-07-19
49348-032-10EA - Each49348-032cf435827-18e6-4e3a-889a-945988f6820512016-07-19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49348-032GENTLE LAXATIVE (BISACODYL) TABLET, DELAYED RELEASE [STRATEGIC SOURCING SERVICES, LLC (SUNMARK)]16Legacy NDC20250411_40a29169-dd77-43b1-8887-b91cf98107c6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49348-032-05493480032051 BLISTER PACK in 1 CARTON (49348-032-05) > 25 TABLET, COATED in 1 BLISTER PACK1 blister pack2002-03-250000-00-00NoNoCurrent
49348-032-1049348003210100 TABLET, COATED in 1 BOTTLE, PLASTIC (49348-032-10) 2002-03-250000-00-00NoNoCurrent