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Digoxin
Digoxin - 53808-0355-1 - (DIGOXIN)
Drug Information of Digoxin
| Product NDC: | 53808-0355 |
| Proprietary Name: | Digoxin |
| Non Proprietary Name: | DIGOXIN |
| Active Ingredient(s): | 250 ug/1 & nbsp; DIGOXIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Digoxin
| Product NDC: | 53808-0355 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077002 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090701 |
Package Information of Digoxin
| Package NDC: | 53808-0355-1 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (53808-0355-1) |
NDC Information of Digoxin
| NDC Code | 53808-0355-1 |
| Proprietary Name | Digoxin |
| Package Description | 30 TABLET in 1 BLISTER PACK (53808-0355-1) |
| Product NDC | 53808-0355 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DIGOXIN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | ANDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | DIGOXIN |
| Strength Number | 250 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient] |
