DocuSol

Product NDC: 17433-9878
11-digit product format: 174339878
Labeler code: 17433
Product ID: 17433-9878_ecfb3572-aff3-375f-e053-2995a90ad328
Type: HUMAN OTC DRUG
Nonproprietary name: docusate sodium
Dosage form: LIQUID
Route: RECTAL
Labeler: Enemeez LLC DBA Summit Pharmaceuticals
Application: part334
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2013-07-08
Marketing end: 2024-10-31
Substance: DOCUSATE SODIUM
Active strength: 283 mg/5mL
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
17433-9878-3	2023-01-13	C162847	48780-1	9d75b9d0-2d8e-f424-e053-dadaa90a57ce	1235366d-b572-3a41-e054-00144ff8d46c
17433-9878-3	2020-01-31	C162847	48780-1	9d75b9d0-2d8e-f424-e053-dadaa90a57ce	1235366d-b572-3a41-e054-00144ff8d46c

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
17433-9878-1	EA - Each	17433-9878	bec574c2-ca74-46b5-bf9a-34ee462aed70	1	2016-01-13
17433-9878-5	EA - Each	17433-9878	3e4b22f5-0f85-42c5-b015-d4c7beb48ad1	1	2013-09-04

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
17433-9878-5	17433987805	5 TUBE in 1 BOX (17433-9878-5) > 5 mL in 1 TUBE (17433-9878-1)	5 tube	2013-07-08	0000-00-00	No	No	Current