Product NDC: | 0054-0057 |
Proprietary Name: | Digoxin |
Non Proprietary Name: | Digoxin |
Active Ingredient(s): | .05 mg/mL & nbsp; Digoxin |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-0057 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021648 |
Marketing Category: | NDA |
Start Marketing Date: | 20040826 |
Package NDC: | 0054-0057-46 |
Package Description: | 60 mL in 1 BOTTLE, DROPPER (0054-0057-46) |
NDC Code | 0054-0057-46 |
Proprietary Name | Digoxin |
Package Description | 60 mL in 1 BOTTLE, DROPPER (0054-0057-46) |
Product NDC | 0054-0057 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Digoxin |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20040826 |
Marketing Category Name | NDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | DIGOXIN |
Strength Number | .05 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient] |