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
- 0904-6748_14fafe89-e4bf-4282-8a72-3bfcee7227fc
- Product NDC
- 0904-6748
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Bisacodyl
- Labeler
- Major Pharmaceuticals
- 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
- 1 BLISTER PACK in 1 CARTON (0904-6748-17) / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 0904-6748-17
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0904-6748-60) · 0904-6748-60
- 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0904-6748-80) · 0904-6748-80
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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