DOCUSATE SODIUM - SENNOSIDES
- Product NDC
- 70000-0229
- 11-digit product format
- 700000229
- Labeler code
- 70000
- Product ID
- 70000-0229_98cf8599-b67f-fc6f-e053-2a95a90ac7ee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DOCUSATE SODIUM - SENNOSIDES
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CARDINAL HEALTH
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-01-27
- Marketing end
- 2019-12-27
- Substance
- DOCUSATE SODIUM; SENNOSIDES
- Active strength
- 50 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record