PlusPHARMA
- Product NDC
- 51645-750
- 11-digit product format
- 516450750
- Labeler code
- 51645
- Product ID
- 51645-750_b3db5c6e-199b-d0ec-e053-2995a90a968c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DOCUSATE SODIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Gemini Pharmaceuticals, Inc. dba Plus Pharma
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2006-03-27
- Marketing end
- 2021-11-30
- Substance
- DOCUSATE SODIUM
- Active strength
- 100 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 |
|---|
| 51645-750-10 | 51645075010 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-750-10) | 2006-03-27 | 2021-11-30 | No | No | Current |