senna
Generic: sennosides
Labeler: h e bDrug Facts
Product Profile
Brand Name
senna
Generic Name
sennosides
Labeler
h e b
Dosage Form
TABLET
Routes
Active Ingredients
sennosides 8.6 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
37808-782
Product ID
37808-782_ffd1f134-7073-471d-9655-fc41a2543490
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2022-02-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808782
Hyphenated Format
37808-782
Supplemental Identifiers
RxCUI
UPC
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
senna (source: ndc)
Generic Name
sennosides (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8.6 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 BOX (37808-782-10) / 100 TABLET in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ffd1f134-7073-471d-9655-fc41a2543490", "openfda": {"upc": ["0041220519132"], "unii": ["3FYP5M0IJX"], "rxcui": ["312935"], "spl_set_id": ["60de7967-279c-478c-b4dd-e3b283375025"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-782-10) / 100 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "37808-782-10", "marketing_start_date": "20220218"}], "brand_name": "Senna", "product_id": "37808-782_ffd1f134-7073-471d-9655-fc41a2543490", "dosage_form": "TABLET", "product_ndc": "37808-782", "generic_name": "Sennosides", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Senna", "active_ingredients": [{"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220218", "listing_expiration_date": "20261231"}