Docusate Sodium
- Product NDC
- 51655-342
- 11-digit product format
- 516550342
- Labeler code
- 51655
- Product ID
- 51655-342_82fb2524-1ae9-3c80-e053-2991aa0a1219
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docusate Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-08-14
- Marketing end
- 0000-00-00
- Substance
- DOCUSATE SODIUM
- Active strength
- 100 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 |
|---|
| 51655-342-20 | Docusate Sodium | 20 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 20 | | 1 |
| 51655-342-52 | Docusate Sodium | 30 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-342 | DOCUSATE SODIUM CAPSULE, LIQUID FILLED [NORTHWIND PHARMACEUTICALS] | 1 | Legacy NDC, 2 package rows | 20190329_82fab9f8-fdf2-fd32-e053-2a91aa0af596.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 51655-342-20 | 51655034220 | 20 in 1 BOTTLE | Historical |
| 51655-342-52 | 51655034252 | 30 in 1 BOTTLE | Historical |