SENNA-S
- Product NDC
- 17714-124
- 11-digit product format
- 177140124
- Labeler code
- 17714
- Product ID
- 17714-124_5cc973b8-e563-2f6c-e053-2a91aa0a9ab8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Senna and Docusate Sodium Tablets, 8.6 mg and 50 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advance Pharmaceutical Inc.
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-02-01
- Marketing end
- 0000-00-00
- Substance
- SENNOSIDES; DOCUSATE SODIUM
- Active strength
- 9 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17714-124-10 | SENNA-S | 1000 in 1 BOTTLE | TABLET | 1000 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17714-124 | SENNA-S (SENNA AND DOCUSATE SODIUM TABLETS, 8.6 MG AND 50 MG) TABLET [ADVANCE PHARMACEUTICAL INC.] | 2 | Legacy NDC, 1 package rows | 20171031_eccac127-5175-4a2e-828d-c9dd87713bb8.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 |
|---|
| 17714-124-10 | 17714012410 | 1000 TABLET in 1 BOTTLE (17714-124-10) | 1000 tablet | 2017-02-01 | 0000-00-00 | No | No | Current |