Product NDC: | 58980-401 |
Proprietary Name: | Vacuant |
Non Proprietary Name: | Docusate Sodium |
Active Ingredient(s): | 283 mg/5mL & nbsp; Docusate Sodium |
Administration Route(s): | RECTAL |
Dosage Form(s): | ENEMA |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58980-401 |
Labeler Name: | Stratus Pharmaceuticals, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110102 |
Package NDC: | 58980-401-05 |
Package Description: | 30 TUBE, WITH APPLICATOR in 1 JAR (58980-401-05) > 5 mL in 1 TUBE, WITH APPLICATOR |
NDC Code | 58980-401-05 |
Proprietary Name | Vacuant |
Package Description | 30 TUBE, WITH APPLICATOR in 1 JAR (58980-401-05) > 5 mL in 1 TUBE, WITH APPLICATOR |
Product NDC | 58980-401 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Docusate Sodium |
Dosage Form Name | ENEMA |
Route Name | RECTAL |
Start Marketing Date | 20110102 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Stratus Pharmaceuticals, Inc |
Substance Name | DOCUSATE SODIUM |
Strength Number | 283 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |