Docusate Sodium, Sennosides
- Product NDC
- 69842-520
- 11-digit product format
- 698420520
- Labeler code
- 69842
- Product ID
- 69842-520_b4548030-7f10-d5b3-e053-2995a90a9b20
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docusate Sodium, Sennosides
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CVS Pharmacy, Inc.
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-07-03
- Marketing end
- 2022-04-30
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69842-520-01 | 69842052001 | 100 TABLET, FILM COATED in 1 BOTTLE (69842-520-01) | 2018-07-03 | 2022-04-30 | No | No | Current |
| 69842-520-04 | 69842052004 | 400 TABLET, FILM COATED in 1 BOTTLE (69842-520-04) | 2018-07-03 | 2022-04-30 | No | No | Current |
| 69842-520-25 | 69842052025 | 250 TABLET, FILM COATED in 1 BOTTLE (69842-520-25) | 2018-07-03 | 2022-04-30 | No | No | Current |