DOK is a Oral Capsule in the Human Otc Drug category. It is labeled and distributed by Redpharm Drug, Inc.. The primary component is Docusate Sodium.
| Product ID | 67296-1556_68165491-0e0d-52d9-e053-2a91aa0ae5f1 |
| NDC | 67296-1556 |
| Product Type | Human Otc Drug |
| Proprietary Name | DOK |
| Generic Name | Dok |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 2018-01-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part334 |
| Labeler Name | RedPharm Drug, Inc. |
| Substance Name | DOCUSATE SODIUM |
| Active Ingredient Strength | 100 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2018-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| DOCUSATE SODIUM | 100 mg/1 |
| SPL SET ID: | 68165491-0e0c-52d9-e053-2a91aa0ae5f1 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0904-2244 | DOK | DOCUSATE SODIUM |
| 0904-5869 | DOK | DOCUSATE SODIUM |
| 0904-6455 | DOK | Docusate Sodium |
| 0904-6457 | DOK | DOCUSATE SODIUM |
| 0904-6458 | DOK | DOCUSATE SODIUM |
| 0904-6750 | DOK | docusate sodium |
| 50090-2842 | DOK | Docusate Sodium |
| 50090-5268 | DOK | DOCUSATE SODIUM |
| 55154-7636 | DOK | Docusate Sodium |
| 55700-719 | DOK | DOCUSATE SODIUM |
| 67296-1556 | DOK | DOK |
| 70518-1531 | DOK | DOCUSATE SODIUM |
| 70518-1983 | DOK | docusate sodium |
| 70518-2105 | DOK | DOCUSATE SODIUM |
| 70934-805 | DOK | DOCUSATE SODIUM |
| 71335-0550 | DOK | DOCUSATE SODIUM |