Docusate Sodium
- Product NDC
- 72789-295
- Requested package NDC
- 72789-295-90
- 11-digit product format
- 727890295
- Labeler code
- 72789
- Product ID
- 72789-295_f082acf2-6258-7499-e053-2995a90ae20d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DOCUSATE SODIUM
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-05-28
- Marketing end
- 0000-00-00
- Substance
- DOCUSATE SODIUM
- Active strength
- 100 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-295 | DOCUSATE SODIUM CAPSULE [PD-RX PHARMACEUTICALS, INC.] | 6 | Legacy NDC | 20240720_2d657c29-c701-4db0-9c06-f680bd921241.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-295-90 | 72789029590 | 90 CAPSULE in 1 BOTTLE, PLASTIC (72789-295-90) | 90 capsule | 2022-12-23 | 0000-00-00 | No | No | Current |