Senna S
- Product NDC
- 10135-669
- 11-digit product format
- 101350669
- Labeler code
- 10135
- Product ID
- 10135-669_441ef4c5-4902-159d-e063-6394a90aebd0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docusate Sodium and Sennosides
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Marlex Pharmaceuticals Inc
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-10-01
- Substance
- DOCUSATE SODIUM; SENNOSIDES
- Active strength
- 50; 8.6 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Senna S
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOCUSATE SODIUM | 50 mg/1 |
| SENNOSIDES | 8.6 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F05Q2T2JA0, 3FYP5M0IJX |
| Rxcui | 998740 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10135-669-01 | Senna S | 100 in 1 BOTTLE | TABLET | 100 | | 6 |
| 10135-669-01 | Senna S | 1 in 1 CARTON | TABLET | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10135-669 | SENNA S (DOCUSATE SODIUM AND SENNOSIDES) TABLET [MARLEX PHARMACEUTICALS INC] | 5 | Current NDC, Legacy NDC, 2 package rows | 20241019_9c87759f-3856-4f30-b5ea-4b37ed90f18c.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 |
|---|
| 10135-669-01 | 10135066901 | 1 BOTTLE in 1 CARTON (10135-669-01) / 100 TABLET in 1 BOTTLE | 1 bottle | 2018-10-01 | 0000-00-00 | No | No | Current |