FDA Application
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NDC Search Results on Active Ingredient: DIGOXIN
Click on Active Ingredient to view the label.
| Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
|---|---|---|---|---|---|
| DIGOXIN | 53808-1006-1 | State of Florida DOH Central Pharmacy | NDA020405 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| DIGOXIN | 17856-0057-5 | Atlantic Biologicals Corps | NDA021648 | HUMAN PRESCRIPTION DRUG | NDA |
| DIGOXIN | 17856-0057-1 | Atlantic Biologicals Corps | NDA021648 | HUMAN PRESCRIPTION DRUG | NDA |
| DIGOXIN | 0054-0057-46 | Hikma Pharmaceuticals USA Inc. | NDA021648 | HUMAN PRESCRIPTION DRUG | NDA |
| 1-30 | 31-60 | 61-90 | 91-120 | 121-150 | 151-154 |
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