DOK
- Product NDC
- 0904-6750
- 11-digit product format
- 009046750
- Labeler code
- 0904
- Product ID
- 0904-6750_08649f2e-5f6c-5ba0-e063-6294a90a5fd1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- docusate sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MAJOR PHARMACEUTICALS
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-06-01
- Substance
- DOCUSATE SODIUM
- Active strength
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DOK
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOCUSATE SODIUM | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F05Q2T2JA0 |
| Rxcui | 1099279, 1483574 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-6750-60 | DOK | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-6750 | DOK (DOCUSATE SODIUM) TABLET [MAJOR PHARMACEUTICALS] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231024_7a92070d-98cc-662f-e053-2991aa0aa1b2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6750-60 | 00904675060 | 100 TABLET in 1 BOTTLE (0904-6750-60) | 100 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |