senna

Generic: senna

Labeler: atlantic biologicals corp.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name senna
Generic Name senna
Labeler atlantic biologicals corp.
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

sennosides a and b 417.12 mg/237mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-8237
Product ID 17856-8237_3b3f526b-e72b-4c6d-e063-6394a90a62e3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M
Listing Expiration 2026-12-31
Marketing Start 2019-10-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178568237
Hyphenated Format 17856-8237

Supplemental Identifiers

RxCUI
702311
UNII
1B5FPI42EN

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 senna (source: ndc)
Application Number M (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 417.12 mg/237mL
source: ndc
Packaging
  • PRINCIPAL PANEL image description image description image description
source: label

Packages (0)

No package records.

Ingredients (1)

sennosides a and b (417.12 mg/237mL)

Linked Drug Pages (1)

SENNA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b3f526b-e72b-4c6d-e063-6394a90a62e3", "openfda": {"unii": ["1B5FPI42EN"], "rxcui": ["702311"], "spl_set_id": ["8b7cc0d5-029b-43f7-a050-8771e7db4551"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [], "brand_name": "SENNA", "product_id": "17856-8237_3b3f526b-e72b-4c6d-e063-6394a90a62e3", "dosage_form": "SYRUP", "product_ndc": "17856-8237", "generic_name": "SENNA", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SENNA", "active_ingredients": [{"name": "SENNOSIDES A AND B", "strength": "417.12 mg/237mL"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191025", "listing_expiration_date": "20261231"}