senexon-s

Generic: docusate sodium 50mg and sennosides 8.6mg

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name senexon-s
Generic Name docusate sodium 50mg and sennosides 8.6mg
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

docusate sodium 50 mg/1, sennosides 8.6 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8331
Product ID 0615-8331_ed210a7f-6612-4caf-851f-c04b02d0cf52
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2019-10-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06158331
Hyphenated Format 0615-8331

Supplemental Identifiers

RxCUI
998740 1248013
UNII
F05Q2T2JA0 3FYP5M0IJX

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name senexon-s (source: ndc)
Generic Name docusate sodium 50mg and sennosides 8.6mg (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 8.6 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-05)
  • 28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-28)
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-39)
source: ndc

Packages (3)

0615-8331-05 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-05) 0615-8331-28 28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-28) 0615-8331-39 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-39)

Ingredients (2)

docusate sodium (50 mg/1) sennosides (8.6 mg/1)

Linked Drug Pages (1)

Senexon-S ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ed210a7f-6612-4caf-851f-c04b02d0cf52", "openfda": {"unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740", "1248013"], "spl_set_id": ["c049ef78-cc16-4209-b553-60cead5c9a80"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-05)", "package_ndc": "0615-8331-05", "marketing_start_date": "20240708"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-28)", "package_ndc": "0615-8331-28", "marketing_start_date": "20241226"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-39)", "package_ndc": "0615-8331-39", "marketing_start_date": "20200107"}], "brand_name": "Senexon-S", "product_id": "0615-8331_ed210a7f-6612-4caf-851f-c04b02d0cf52", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0615-8331", "generic_name": "Docusate Sodium 50mg and Sennosides 8.6mg", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Senexon-S", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191002", "listing_expiration_date": "20261231"}