United States · FDA National Drug Code directory

Sennosides

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
71335-2660_644bf13d-7b0c-4042-b8a2-d017af5ab911
Product NDC
71335-2660
Form
TABLET, FILM COATED
Composition / generic term
Sennosides
Labeler
Bryant Ranch Prepack
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20220517
Source listing expiry
20261231

Source-listed ingredients

  • SENNOSIDES — 8.6 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-2660-1) · 71335-2660-1
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-2660-2) · 71335-2660-2
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-2660-3) · 71335-2660-3
  • 56 TABLET, FILM COATED in 1 BOTTLE (71335-2660-4) · 71335-2660-4
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-2660-5) · 71335-2660-5
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-2660-6) · 71335-2660-6
  • 10 TABLET, FILM COATED in 1 BOTTLE (71335-2660-7) · 71335-2660-7

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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