Product NDC: | 53807-216 |
Proprietary Name: | Docusate Sodium Liquid |
Non Proprietary Name: | Docusate sodium |
Active Ingredient(s): | 10 mg/mL & nbsp; Docusate sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53807-216 |
Labeler Name: | Rij Pharmaceutical Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19990316 |
Package NDC: | 53807-216-08 |
Package Description: | 236 mL in 1 BOTTLE, PLASTIC (53807-216-08) |
NDC Code | 53807-216-08 |
Proprietary Name | Docusate Sodium Liquid |
Package Description | 236 mL in 1 BOTTLE, PLASTIC (53807-216-08) |
Product NDC | 53807-216 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Docusate sodium |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19990316 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Rij Pharmaceutical Corporation |
Substance Name | DOCUSATE SODIUM |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes |