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PURGASOL
PURGASOL - 24286-1552-6 - (Sennosides Docusate Sodium)
Drug Information of PURGASOL
| Product NDC: | 24286-1552 |
| Proprietary Name: | PURGASOL |
| Non Proprietary Name: | Sennosides Docusate Sodium |
| Active Ingredient(s): | 50; 8.6 mg/1; mg/1 & nbsp; Sennosides Docusate Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PURGASOL
| Product NDC: | 24286-1552 |
| Labeler Name: | DLC Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091116 |
Package Information of PURGASOL
| Package NDC: | 24286-1552-6 |
| Package Description: | 1 BOTTLE in 1 BOX (24286-1552-6) > 60 TABLET in 1 BOTTLE |
NDC Information of PURGASOL
| NDC Code | 24286-1552-6 |
| Proprietary Name | PURGASOL |
| Package Description | 1 BOTTLE in 1 BOX (24286-1552-6) > 60 TABLET in 1 BOTTLE |
| Product NDC | 24286-1552 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sennosides Docusate Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091116 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DLC Laboratories, Inc. |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
