NDC 0904-6724

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 Major Pharmaceuticals. The primary component is Sennosides; Docusate Sodium.

Product ID0904-6724_780b838c-b1fa-442f-e053-2991aa0a7758
NDC0904-6724
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 NameMajor Pharmaceuticals
Substance NameSENNOSIDES; DOCUSATE SODIUM
Active Ingredient Strength9 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0904-6724-61

10 BLISTER PACK in 1 BOX (0904-6724-61) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2019-03-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0904-6724-61 [00904672461]

Sennosides,Docusate sodium TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart334
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2019-03-14

Drug Details

Active Ingredients

IngredientStrength
SENNOSIDES8.6 mg/1

OpenFDA Data

SPL SET ID:780b838c-b1f9-442f-e053-2991aa0a7758
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 998740
    • UPC Code
  • 0309046724612

    • 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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