| Product NDC: | 54838-107 |
| Proprietary Name: | Silace |
| Non Proprietary Name: | Docusate sodium |
| Active Ingredient(s): | 60 mg/15mL & nbsp; Docusate sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54838-107 |
| Labeler Name: | Silarx Pharmaceuticals,Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19900305 |
| Package NDC: | 54838-107-80 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (54838-107-80) |
| NDC Code | 54838-107-80 |
| Proprietary Name | Silace |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (54838-107-80) |
| Product NDC | 54838-107 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Docusate sodium |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 19900305 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Silarx Pharmaceuticals,Inc |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 60 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes |