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DOCUSATE SODIUM
DOCUSATE SODIUM - 60258-955-01 - (Docusate Sodium)
Drug Information of DOCUSATE SODIUM
| Product NDC: | 60258-955 |
| 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: | 60258-955 |
| Labeler Name: | Cypress Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20000801 |
Package Information of DOCUSATE SODIUM
| Package NDC: | 60258-955-01 |
| Package Description: | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (60258-955-01) |
NDC Information of DOCUSATE SODIUM
| NDC Code | 60258-955-01 |
| Proprietary Name | DOCUSATE SODIUM |
| Package Description | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (60258-955-01) |
| Product NDC | 60258-955 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Docusate Sodium |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20000801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Cypress Pharmaceuticals, Inc. |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
