Docusate Sodium

Product NDC
0904-7115
11-digit product format
009047115
Labeler code
0904
Product ID
0904-7115_100f18be-911a-4a77-9b5d-2ff48dd3c4ce
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate Sodium
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Major Pharmaceuticals
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-04-16
Marketing end
0000-00-00
Substance
DOCUSATE SODIUM
Active strength
100 mg/1
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
0904-7115-61EA - Each0904-711513c8fa70-0045-4950-a8b5-337e543a208a12021-07-15

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0904-7115-610090471156110 BLISTER PACK in 1 CARTON (0904-7115-61) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK10 blister pack2021-04-160000-00-00NoNoCurrent