DOCUSATE SENNOSIDES
- Product NDC
- 61919-771
- 11-digit product format
- 619190771
- Labeler code
- 61919
- Product ID
- 61919-771_98ce8a4c-48df-b65a-e053-2995a90a123c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DOCUSATE SENNOSIDES
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DIRECTRX
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-04-29
- Marketing end
- 0000-00-00
- Substance
- DOCUSATE SODIUM; SENNOSIDES A AND B
- Active strength
- 50 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-771-60 | 61919077160 | 60 TABLET, FILM COATED in 1 BOTTLE (61919-771-60) | 2019-04-29 | 0000-00-00 | No | No | Current |