Product NDC: | 68210-0402 |
Proprietary Name: | DOCUSATE SODIUM |
Non Proprietary Name: | DOCUSATE SODIUM |
Active Ingredient(s): | 50 mg/1 & nbsp; DOCUSATE SODIUM |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68210-0402 |
Labeler Name: | SPIRIT PHARMACEUTICALS,LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part310.545 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091001 |
Package NDC: | 68210-0402-1 |
Package Description: | 1 BAG in 1 BOX (68210-0402-1) > 10 CAPSULE, LIQUID FILLED in 1 BAG |
NDC Code | 68210-0402-1 |
Proprietary Name | DOCUSATE SODIUM |
Package Description | 1 BAG in 1 BOX (68210-0402-1) > 10 CAPSULE, LIQUID FILLED in 1 BAG |
Product NDC | 68210-0402 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DOCUSATE SODIUM |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20091001 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | SPIRIT PHARMACEUTICALS,LLC |
Substance Name | DOCUSATE SODIUM |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes |