Pedia-Lax

Product NDC
0132-0106
11-digit product format
001320106
Labeler code
0132
Product ID
0132-0106_e8816dce-8c24-4e27-9a41-b64eecb0497a
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate Sodium
Dosage form
LIQUID
Route
ORAL
Labeler
C.B. Fleet Company, Inc.
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2008-03-01
Marketing end
0000-00-00
Substance
DOCUSATE SODIUM
Active strength
50 mg/15mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0132-0106-24ML - Milliliter0132-0106baf7e618-44ab-49aa-a963-1aa1bd902fbc12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0132-0106-2400132010624118 mL in 1 CARTON (0132-0106-24) 118 ml2008-03-010000-00-00NoNoCurrent