Bisacodyl
- Product NDC
- 41226-003
- 11-digit product format
- 412260003
- Labeler code
- 41226
- Product ID
- 41226-003_2dc61a4e-5307-5145-e063-6294a90a06d7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bisacodyl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- KROGER COMPANY
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-06-01
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bisacodyl
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISACODYL | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 10X0709Y6I |
| Rxcui | 308753 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41226-003-52 | Bisacodyl | 25 in 1 BLISTER PACK | TABLET, COATED | 25 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41226-003 | BISACODYL TABLET, COATED [KROGER COMPANY] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250212_a13a8eec-3652-8c57-e053-2995a90aaebf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41226-003-52 | 41226000352 | 25 TABLET, COATED in 1 BLISTER PACK (41226-003-52) | 2020-06-01 | 0000-00-00 | No | No | Current |