DOCUSATE SODIUM
- Product NDC
- 68071-3438
- 11-digit product format
- 680713438
- Labeler code
- 68071
- Product ID
- 68071-3438_0919f0ef-9139-b605-e063-6294a90af582
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DOCUSATE SODIUM
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-11-15
- Substance
- DOCUSATE SODIUM
- Active strength
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F05Q2T2JA0 | DOCUSATE SODIUM | 577-11-7 | DOCUSATE SODIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3438-3 | 68071343803 | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (68071-3438-3) | 2023-06-12 | No | No | Historical |
| 68071-3438-6 | 68071343806 | 60 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (68071-3438-6) | 2023-06-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| DRUG FACTS | NuCare Pharmaceuticals,Inc. | 2024-11-01 | HUMAN OTC DRUG LABEL | 2 |