Plus Pharma Senna Plus

Product NDC: 51645-850
11-digit product format: 516450850
Labeler code: 51645
Product ID: 51645-850_b3db6ed6-cbc5-d23a-e053-2995a90ad052
Type: HUMAN OTC DRUG
Nonproprietary name: DOCUSATE SODIUM,SENNOSIDES
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Gemini Pharmaceuticals, Inc. dba Plus Pharma
Application: part334
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2006-03-27
Marketing end: 2022-03-31
Substance: DOCUSATE SODIUM; SENNOSIDES
Active strength: 50 mg/1; mg/1
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
998740	sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet	PSN	9adcfb31-33b9-6b70-e053-2995a90af3eb	1
998740	docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SCD	9adcfb31-33b9-6b70-e053-2995a90af3eb	1
998740	DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SY	9adcfb31-33b9-6b70-e053-2995a90af3eb	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
51645-850-06	51645085006	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-850-06)	2006-03-27	2022-03-31	No	No	Current