Docusate Sodium

Product NDC
63739-089
11-digit product format
637390089
Labeler code
63739
Product ID
63739-089_62c8ffe5-321f-4747-ad38-db2c54a393ae
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate Sodium
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
McKesson Packaging Services Business Unit of McKesson Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2004-12-01
Marketing end
0000-00-00
Substance
DOCUSATE SODIUM
Active strength
100 mg/1
NDC exclude flag
E
Listing certified through
2018-12-31
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
63739-089-03EA - Each63739-08909e05717-e1ea-464a-95d9-11d2c24b356f12012-07-24
63739-089-10EA - Each63739-08945ad82f9-f4a1-4187-b3dc-ed4956c2728712012-07-24