Bisacodyl
- Product NDC
- 68210-3120
- Requested package NDC
- 68210-3120-2
- 11-digit product format
- 682103120
- Labeler code
- 68210
- Product ID
- 68210-3120_ee8b0470-050f-df27-e053-2995a90a2601
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bisacodyl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Spirit Pharmaceuticals LLC
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-11
- Marketing end
- 0000-00-00
- Substance
- BISACODYL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Stimulant Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68210-3120-2 | 68210312002 | 1 BOTTLE in 1 CARTON (68210-3120-2) > 25 TABLET in 1 BOTTLE | 1 bottle | 2020-03-11 | 0000-00-00 | No | No | Current |