Bisacodyl Laxative
- Product NDC
- 50804-190
- 11-digit product format
- 508040190
- Labeler code
- 50804
- Product ID
- 50804-190_d8b6d34f-daaf-4f9c-8f08-e5e75e8c6c63
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bisacodyl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Good Sense (Geiss, Destin & Dunn, Inc.)
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-07-16
- Marketing end
- 2025-01-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50804-190-03 | 50804019003 | 1 BLISTER PACK in 1 CARTON (50804-190-03) > 25 TABLET, COATED in 1 BLISTER PACK | 1 blister pack | 2010-07-16 | 0000-00-00 | No | No | Current |