United States · FDA National Drug Code directory
Senokot
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
- 67618-120_8319c8b6-8d3f-416d-a864-39cb879df2da
- Product NDC
- 67618-120
- Form
- TABLET, FILM COATED
- Composition / generic term
- standardized senna concentrate
- Labeler
- Atlantis Consumer Healthcare, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 19880901
- Source listing expiry
- 20261231
Source-listed ingredients
- SENNOSIDES — 17.2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 36 TABLET, FILM COATED in 1 BOTTLE (67618-120-06) · 67618-120-06
- 1 BLISTER PACK in 1 CARTON (67618-120-12) / 12 TABLET, FILM COATED in 1 BLISTER PACK · 67618-120-12
- 2 CARTON in 1 PACKAGE (67618-120-72) / 1 BOTTLE in 1 CARTON / 36 TABLET, FILM COATED in 1 BOTTLE · 67618-120-72
- 72 TABLET, FILM COATED in 1 BOTTLE (67618-120-73) · 67618-120-73
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →