sennosides and docusate sodium

Generic: sennosides, docusate sodium

Labeler: asclemed usa, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sennosides and docusate sodium
Generic Name sennosides, docusate sodium
Labeler asclemed usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-918
Product ID 76420-918_2d9d8f71-cc36-459a-e063-6394a90acf8e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2020-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420918
Hyphenated Format 76420-918

Supplemental Identifiers

RxCUI
998740
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 sennosides and docusate sodium (source: ndc)
Generic Name sennosides, docusate sodium (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 8.6 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (76420-918-01)
  • 30 TABLET in 1 BOTTLE (76420-918-30)
  • 60 TABLET in 1 BOTTLE (76420-918-60)
  • 90 TABLET in 1 BOTTLE (76420-918-90)
source: ndc

Packages (4)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d9d8f71-cc36-459a-e063-6394a90acf8e", "openfda": {"unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["2db546de-20dc-4697-aff2-12471f073b1d"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-918-01)", "package_ndc": "76420-918-01", "marketing_start_date": "20250208"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-918-30)", "package_ndc": "76420-918-30", "marketing_start_date": "20250208"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-918-60)", "package_ndc": "76420-918-60", "marketing_start_date": "20250208"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-918-90)", "package_ndc": "76420-918-90", "marketing_start_date": "20250208"}], "brand_name": "Sennosides and Docusate Sodium", "product_id": "76420-918_2d9d8f71-cc36-459a-e063-6394a90acf8e", "dosage_form": "TABLET", "product_ndc": "76420-918", "generic_name": "Sennosides, Docusate Sodium", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sennosides and Docusate Sodium", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}