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
- 68016-688_12bba10e-970d-443e-93fe-796395cc7093
- Product NDC
- 68016-688
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Bisacodyl
- Labeler
- Chain Drug Consortium
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20020325 / 20270131
Source-listed ingredients
- BISACODYL — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (68016-688-10) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC · 68016-688-10
- 1 BLISTER PACK in 1 CARTON (68016-688-25) / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 68016-688-25
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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