Product NDC: | 58118-7889 |
Proprietary Name: | MAJOR DOK Docusate Sodium |
Non Proprietary Name: | DOCUSATE SODIUM |
Active Ingredient(s): | 100 mg/1 & nbsp; DOCUSATE SODIUM |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58118-7889 |
Labeler Name: | Clinical Solutions Wholesale |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100423 |
Package NDC: | 58118-7889-0 |
Package Description: | 1 CAPSULE, LIQUID FILLED in 1 PACKET (58118-7889-0) |
NDC Code | 58118-7889-0 |
Proprietary Name | MAJOR DOK Docusate Sodium |
Package Description | 1 CAPSULE, LIQUID FILLED in 1 PACKET (58118-7889-0) |
Product NDC | 58118-7889 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DOCUSATE SODIUM |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20100423 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Clinical Solutions Wholesale |
Substance Name | DOCUSATE SODIUM |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes |