docusate sodium and sennosides

Generic: docusate sodium and sennosides

Labeler: softgel healthcare private limited
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name docusate sodium and sennosides
Generic Name docusate sodium and sennosides
Labeler softgel healthcare private limited
Dosage Form CAPSULE, GELATIN COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
SOFTGEL HEALTHCARE PRIVATE LIMITED

Identifiers & Regulatory

Product NDC 35916-0453
Product ID 35916-0453_47dbd4d5-5093-0741-e063-6294a90a001a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2027-12-31
Marketing Start 2024-06-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 359160453
Hyphenated Format 35916-0453

Supplemental Identifiers

RxCUI
1791612
UPC
0335916045310
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 docusate sodium and sennosides (source: ndc)
Generic Name docusate sodium and sennosides (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 8.6 mg/1
source: ndc
Packaging
  • 500 CAPSULE, GELATIN COATED in 1 BOTTLE (35916-0453-1)
  • 2 POUCH in 1 BOX (35916-0453-3) / 3000 CAPSULE, GELATIN COATED in 1 POUCH
source: ndc

Packages (2)

35916-0453-1 500 CAPSULE, GELATIN COATED in 1 BOTTLE (35916-0453-1) 35916-0453-3 2 POUCH in 1 BOX (35916-0453-3) / 3000 CAPSULE, GELATIN COATED in 1 POUCH

Ingredients (2)

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

Linked Drug Pages (1)

Docusate Sodium and Sennosides ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47dbd4d5-5093-0741-e063-6294a90a001a", "openfda": {"upc": ["0335916045310"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["1791612"], "spl_set_id": ["19830f9a-27b1-910d-e063-6294a90adace"], "manufacturer_name": ["SOFTGEL HEALTHCARE PRIVATE LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, GELATIN COATED in 1 BOTTLE (35916-0453-1)", "package_ndc": "35916-0453-1", "marketing_start_date": "20240604"}, {"sample": false, "description": "2 POUCH in 1 BOX (35916-0453-3)  / 3000 CAPSULE, GELATIN COATED in 1 POUCH", "package_ndc": "35916-0453-3", "marketing_start_date": "20250612"}], "brand_name": "Docusate Sodium and Sennosides", "product_id": "35916-0453_47dbd4d5-5093-0741-e063-6294a90a001a", "dosage_form": "CAPSULE, GELATIN COATED", "product_ndc": "35916-0453", "generic_name": "Docusate Sodium and Sennosides", "labeler_name": "SOFTGEL HEALTHCARE PRIVATE LIMITED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Docusate Sodium and Sennosides", "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": "20240604", "listing_expiration_date": "20271231"}