Docusate Sodium
- Product NDC
- 69160-002
- 11-digit product format
- 691600002
- Labeler code
- 69160
- Product ID
- 69160-002_af46cd98-9404-fb02-e053-2a95a90a27f3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- docusate sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Olds Softgels Inc.
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-05-19
- Marketing end
- 0000-00-00
- Substance
- DOCUSATE SODIUM
- Active strength
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 69160-002-01 | Docusate Sodium | 18000 in 1 BOX | TABLET | 18000 | | 4 |
| 69160-002-03 | Docusate Sodium | 1000 in 1 BOTTLE | TABLET | 1000 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69160-002 | DOCUSATE SODIUM TABLET [OLDS SOFTGELS INC.] | 4 | Legacy NDC, 2 package rows | 20200915_166898e7-829e-42fb-8266-9b487cfe7dd0.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 |
|---|
| 69160-002-01 | 69160000201 | 18000 TABLET in 1 BOX (69160-002-01) | 18000 tablet | 2015-05-19 | 0000-00-00 | No | No | Current |
| 69160-002-03 | 69160000203 | 1000 TABLET in 1 BOTTLE (69160-002-03) | 1000 tablet | 2015-05-19 | 0000-00-00 | No | No | Current |