SENNA-S
- Product NDC
- 68210-3002
- Requested package NDC
- 68210-3002-0
- 11-digit product format
- 682103002
- Labeler code
- 68210
- Product ID
- 68210-3002_ee50b653-def5-7696-e053-2995a90a9026
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DOCUSATE SODIUM AND SENNOSIDES
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- SPIRIT PHARMACEUTICALS LLC
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-04-17
- Marketing end
- 0000-00-00
- Substance
- DOCUSATE SODIUM; SENNOSIDES
- Active strength
- 50 mg/1; mg/1
- 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.
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 |
|---|
| 68210-3002-0 | SENNA-S | 60 in 1 BOTTLE | TABLET | 60 | | 7 |
| 68210-3002-0 | SENNA-S | 1 in 1 CARTON | TABLET | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68210-3002 | SENNA-S (DOCUSATE SODIUM AND SENNOSIDES) TABLET [SPIRIT PHARMACEUTICALS LLC] | 7 | Legacy NDC, 2 package rows | 20241213_136fa35c-26ce-49ad-853d-c586e9cf3fe1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68210-3002-0 | 68210300200 | 1 BOTTLE in 1 CARTON (68210-3002-0) > 60 TABLET in 1 BOTTLE | 1 bottle | 2018-04-17 | 0000-00-00 | No | No | Current |