United States · FDA National Drug Code directory

Bisacodyl

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
71335-2010_42ebd7ff-4d1b-4c81-9374-43cbef0dad3a
Product NDC
71335-2010
Form
TABLET, DELAYED RELEASE
Composition / generic term
Bisacodyl
Labeler
Bryant Ranch Prepack
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20181201
Source listing expiry
20261231

Source-listed ingredients

  • BISACODYL — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 25 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-0) · 71335-2010-0
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-1) · 71335-2010-1
  • 2 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-2) · 71335-2010-2
  • 3 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-3) · 71335-2010-3
  • 4 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-4) · 71335-2010-4
  • 10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-5) · 71335-2010-5
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-6) · 71335-2010-6
  • 8 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-7) · 71335-2010-7
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-8) · 71335-2010-8
  • 20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-9) · 71335-2010-9

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 →