sennosides
Generic: sennosides
Labeler: granules usa incDrug Facts
Product Profile
Brand Name
sennosides
Generic Name
sennosides
Labeler
granules usa inc
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
sennosides 17.2 mg/17.21
Manufacturer
Identifiers & Regulatory
Product NDC
69848-016
Product ID
69848-016_468e82c6-8c4a-672c-e063-6394a90a5f0e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2020-05-29
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69848016
Hyphenated Format
69848-016
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 (source: ndc)
Generic Name
sennosides (source: ndc)
Application Number
M007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 17.2 mg/17.21
Packaging
- 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (69848-016-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "468e82c6-8c4a-672c-e063-6394a90a5f0e", "openfda": {"unii": ["3FYP5M0IJX"], "rxcui": ["2169295"], "spl_set_id": ["a619b8f4-1b5d-181b-e053-2995a90ab729"], "manufacturer_name": ["Granules USA Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, LIQUID FILLED in 1 BOTTLE (69848-016-10)", "package_ndc": "69848-016-10", "marketing_start_date": "20200529"}], "brand_name": "Sennosides", "product_id": "69848-016_468e82c6-8c4a-672c-e063-6394a90a5f0e", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "69848-016", "generic_name": "Sennosides", "labeler_name": "Granules USA Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sennosides", "active_ingredients": [{"name": "SENNOSIDES", "strength": "17.2 mg/17.21"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200529", "listing_expiration_date": "20261231"}