Bisacodyl
- Product NDC
- 30142-191
- 11-digit product format
- 301420191
- Labeler code
- 30142
- Product ID
- 30142-191_c4dd2e48-ab73-4dd7-89b3-d5248b55be7c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bisacodyl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- The Kroger Co.
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-12-30
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30142-191-01 | 30142019101 | 4 BLISTER PACK in 1 CARTON (30142-191-01) > 25 TABLET, COATED in 1 BLISTER PACK | 4 blister pack | 2013-12-30 | 0000-00-00 | No | No | Current |
| 30142-191-03 | 30142019103 | 1 BLISTER PACK in 1 CARTON (30142-191-03) > 25 TABLET, COATED in 1 BLISTER PACK | 1 blister pack | 2013-12-30 | 0000-00-00 | No | No | Current |