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Sennosides and Docusate Sodium
Sennosides and Docusate Sodium - 63739-432-04 - (Sennosides and Docusate Sodium)
Drug Information of Sennosides and Docusate Sodium
| Product NDC: | 63739-432 |
| Proprietary Name: | Sennosides and Docusate Sodium |
| Non Proprietary Name: | Sennosides and Docusate Sodium |
| Active Ingredient(s): | 50; 8.6 mg/1; mg/1 & nbsp; Sennosides and Docusate Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sennosides and Docusate Sodium
| Product NDC: | 63739-432 |
| Labeler Name: | McKesson Packaging Services a business unit of McKesson Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20071011 |
Package Information of Sennosides and Docusate Sodium
| Package NDC: | 63739-432-04 |
| Package Description: | 25 BLISTER PACK in 1 BOX (63739-432-04) > 30 TABLET in 1 BLISTER PACK |
NDC Information of Sennosides and Docusate Sodium
| NDC Code | 63739-432-04 |
| Proprietary Name | Sennosides and Docusate Sodium |
| Package Description | 25 BLISTER PACK in 1 BOX (63739-432-04) > 30 TABLET in 1 BLISTER PACK |
| Product NDC | 63739-432 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sennosides and Docusate Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20071011 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | McKesson Packaging Services a business unit of McKesson Corporation |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
