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Digoxin
Digoxin - 0641-1410-35 - (Digoxin)
Drug Information of Digoxin
| Product NDC: | 0641-1410 |
| Proprietary Name: | Digoxin |
| Non Proprietary Name: | Digoxin |
| Active Ingredient(s): | .25 mg/mL & nbsp; Digoxin |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Digoxin
| Product NDC: | 0641-1410 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083391 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19751024 |
Package Information of Digoxin
| Package NDC: | 0641-1410-35 |
| Package Description: | 25 AMPULE in 1 CARTON (0641-1410-35) > 2 mL in 1 AMPULE (0641-1410-31) |
NDC Information of Digoxin
| NDC Code | 0641-1410-35 |
| Proprietary Name | Digoxin |
| Package Description | 25 AMPULE in 1 CARTON (0641-1410-35) > 2 mL in 1 AMPULE (0641-1410-31) |
| Product NDC | 0641-1410 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Digoxin |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19751024 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | DIGOXIN |
| Strength Number | .25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient] |
