Docusate Sodium
- Product NDC
- 71335-1133
- 11-digit product format
- 713351133
- Labeler code
- 71335
- Product ID
- 71335-1133_945e327e-e05a-4fcc-9aa6-70ac50f3200a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Stool Softener
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-05-01
- Marketing end
- 0000-00-00
- Substance
- DOCUSATE SODIUM
- Active strength
- 250 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 71335-1133-1 | 71335113301 | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-1133-1) | 2019-03-11 | 0000-00-00 | No | No | Current |
| 71335-1133-2 | 71335113302 | 60 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-1133-2) | 2019-03-11 | 0000-00-00 | No | No | Current |
| 71335-1133-3 | 71335113303 | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-1133-3) | 2019-03-11 | 0000-00-00 | No | No | Current |
| 71335-1133-4 | 71335113304 | 7 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-1133-4) | 2019-03-11 | 0000-00-00 | No | No | Current |