NDC 0615-8276

Sennosides,Docusate sodium

Sennosides,docusate Sodium

Sennosides,Docusate sodium is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Ncs Healthcare Of Ky, Inc Dba Vangard Labs. The primary component is Docusate Sodium; Sennosides.

Product ID0615-8276_18c8eeff-7363-471b-834a-85ff04d211b4
NDC0615-8276
Product TypeHuman Otc Drug
Proprietary NameSennosides,Docusate sodium
Generic NameSennosides,docusate Sodium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2018-12-20
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart334
Labeler NameNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameDOCUSATE SODIUM; SENNOSIDES
Active Ingredient Strength50 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0615-8276-39

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8276-39)
Marketing Start Date2019-02-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0615-8276-39 [00615827639]

Sennosides,Docusate sodium TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart334
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-02-22

Drug Details

Active Ingredients

IngredientStrength
DOCUSATE SODIUM50 mg/1

OpenFDA Data

SPL SET ID:17d590a7-6698-497f-a35e-50c51d432726
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 998740

    • NDC Crossover Matching brand name "Sennosides,Docusate sodium" or generic name "Sennosides,docusate Sodium"

    NDCBrand NameGeneric Name
    0536-1169Sennosides,Docusate sodiumSennosides,Docusate sodium
    0615-8276Sennosides,Docusate sodiumSennosides,Docusate sodium
    0904-6724Sennosides,Docusate sodiumSennosides,Docusate sodium
    55154-7299Sennosides,Docusate sodiumSennosides,Docusate sodium
    70518-1885Sennosides,Docusate sodiumSennosides,Docusate sodium
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