BISACODYL
- Product NDC
- 84324-132
- 11-digit product format
- 843240132
- Labeler code
- 84324
- Product ID
- 84324-132_a6a9f66a-c928-4960-90c2-e4b56d496153
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BISACODYL
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NUVICARE LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-02
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BISACODYL
- Listing expiration
- 2027-12-31
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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84324-132-01 | BISACODYL | 100 in 1 BOTTLE | TABLET, COATED | 100 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 84324-132-01 | 84324013201 | 100 TABLET, COATED in 1 BOTTLE (84324-132-01) | 2026-03-02 | No | No | Current |