Docusate Sodium

Product NDC: 48433-101
11-digit product format: 484330101
Labeler code: 48433
Product ID: 48433-101_3c42dd05-b2d9-411b-8ef2-63baa98ebe3b
Type: HUMAN OTC DRUG
Nonproprietary name: Docusate Sodium
Dosage form: CAPSULE, LIQUID FILLED
Route: ORAL
Labeler: Safecor Health, LLC
Application: part334
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2000-05-01
Marketing end: 0000-00-00
Substance: DOCUSATE SODIUM
Active strength: 250 mg/1
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48433-101-01	2022-01-30	C162847	48780-1	d6a99b39-8552-a426-e053-dadaa90af4c2	a2586a38-4e2c-4244-8618-0b614d585605
48433-101-01	2022-01-28	C162847	48780-1	d6a99b39-8552-a426-e053-dadaa90af4c2	a2586a38-4e2c-4244-8618-0b614d585605

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
48433-101-01	EA - Each	48433-101	16ee84a5-74e3-4827-aa0e-cd573b1b801f	1	2016-05-16

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
48433-101-01	48433010101	100 CAPSULE, LIQUID FILLED in 1 BOX, UNIT-DOSE (48433-101-01)	2000-05-01	0000-00-00	No	No	Current