senna-s

Generic: docusate sodium, sennosides

Labeler: granulation technology, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name senna-s
Generic Name docusate sodium, sennosides
Labeler granulation technology, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Granulation Technology, Inc.

Identifiers & Regulatory

Product NDC 63561-0187
Product ID 63561-0187_3b28e1ec-d284-2f66-e063-6294a90aa7f1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2025-07-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 635610187
Hyphenated Format 63561-0187

Supplemental Identifiers

RxCUI
998740
UPC
0363561018731
UNII
F05Q2T2JA0 3FYP5M0IJX

Packaging Origin

Original Packager
true

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 senna-s (source: ndc)
Generic Name docusate sodium, sennosides (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
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-1)
  • 220 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-2)
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-3)
source: ndc

Packages (3)

63561-0187-1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-1) 63561-0187-2 220 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-2) 63561-0187-3 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-3)

Ingredients (2)

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

Linked Drug Pages (1)

Senna-S ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b28e1ec-d284-2f66-e063-6294a90aa7f1", "openfda": {"upc": ["0363561018731"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["f36c509e-b93b-4d7f-a18a-41e585369a15"], "manufacturer_name": ["Granulation Technology, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-1)", "package_ndc": "63561-0187-1", "marketing_start_date": "20250729"}, {"sample": false, "description": "220 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-2)", "package_ndc": "63561-0187-2", "marketing_start_date": "20250729"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-3)", "package_ndc": "63561-0187-3", "marketing_start_date": "20250729"}], "brand_name": "Senna-S", "product_id": "63561-0187_3b28e1ec-d284-2f66-e063-6294a90aa7f1", "dosage_form": "TABLET, FILM COATED", "product_ndc": "63561-0187", "generic_name": "DOCUSATE SODIUM, SENNOSIDES", "labeler_name": "Granulation Technology, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Senna-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": "20250729", "listing_expiration_date": "20261231"}