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Docusate Sodium
Docusate Sodium - 63739-478-01 - (Docusate Sodium)
Drug Information of Docusate Sodium
| Product NDC: | 63739-478 |
| Proprietary Name: | Docusate Sodium |
| Non Proprietary Name: | Docusate Sodium |
| Active Ingredient(s): | 100 mg/1 & nbsp; Docusate Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Docusate Sodium
| Product NDC: | 63739-478 |
| Labeler Name: | McKesson Packaging Services Business Unit of McKesson Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101108 |
Package Information of Docusate Sodium
| Package NDC: | 63739-478-01 |
| Package Description: | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-478-01) > 30 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of Docusate Sodium
| NDC Code | 63739-478-01 |
| Proprietary Name | Docusate Sodium |
| Package Description | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-478-01) > 30 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 63739-478 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Docusate Sodium |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20101108 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | McKesson Packaging Services Business Unit of McKesson Corporation |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
