Product NDC: | 0536-0590 |
Proprietary Name: | Diocto |
Non Proprietary Name: | Docusate Sodium |
Active Ingredient(s): | 50 mg/5mL & nbsp; Docusate Sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0536-0590 |
Labeler Name: | The Harvard Drug Group, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130301 |
Package NDC: | 0536-0590-85 |
Package Description: | 473 mL in 1 BOTTLE (0536-0590-85) |
NDC Code | 0536-0590-85 |
Proprietary Name | Diocto |
Package Description | 473 mL in 1 BOTTLE (0536-0590-85) |
Product NDC | 0536-0590 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Docusate Sodium |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20130301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | The Harvard Drug Group, LLC |
Substance Name | DOCUSATE SODIUM |
Strength Number | 50 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |