Stool Softener

Product NDC
71335-0632
11-digit product format
713350632
Labeler code
71335
Product ID
71335-0632_7ff5b843-e930-4718-804b-c6e0d555b29d
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate Sodium
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-01-31
Marketing end
0000-00-00
Substance
DOCUSATE SODIUM
Active strength
250 mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-0632-2EA - Each71335-0632aff633b6-b326-4f66-aeb6-695637ce445512018-08-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0632-17133506320130 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0632-1) 2018-01-030000-00-00NoNoCurrent
71335-0632-27133506320260 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0632-2) 2018-01-030000-00-00NoNoCurrent
71335-0632-371335063203100 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0632-3) 2018-01-030000-00-00NoNoCurrent
71335-0632-4713350632047 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0632-4) 2018-01-030000-00-00NoNoCurrent