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
- 0904-6407_e4f6f4a5-584f-41fc-a279-a0cb3474c2e9
- Product NDC
- 0904-6407
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Bisacodyl
- Labeler
- Major Pharmaceuticals
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20020325
- Source listing expiry
- 20271231
Source-listed ingredients
- BISACODYL — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 BOX (0904-6407-61) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 0904-6407-61
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 →