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Stool Softener
Stool Softener - 63548-4000-1 - (Docusate Sodium and Sennosides)
Drug Information of Stool Softener
| Product NDC: | 63548-4000 |
| Proprietary Name: | Stool Softener |
| Non Proprietary Name: | Docusate Sodium and Sennosides |
| Active Ingredient(s): | 50; 8.6 mg/1; mg/1 & nbsp; Docusate Sodium and Sennosides |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Stool Softener
| Product NDC: | 63548-4000 |
| Labeler Name: | Avema Pharma Solutions |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100102 |
Package Information of Stool Softener
| Package NDC: | 63548-4000-1 |
| Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (63548-4000-1) |
NDC Information of Stool Softener
| NDC Code | 63548-4000-1 |
| Proprietary Name | Stool Softener |
| Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (63548-4000-1) |
| Product NDC | 63548-4000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Docusate Sodium and Sennosides |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100102 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Avema Pharma Solutions |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
