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 | 68071-3011-9 | NuCare Pharmaceuticals, Inc. | NDA020405 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DIGOXIN | 68071-3011-3 | NuCare Pharmaceuticals, Inc. | NDA020405 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DIGOXIN | 68071-3011-7 | NuCare Pharmaceuticals, Inc. | NDA020405 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DIGOXIN | 53808-1006-1 | State of Florida DOH Central Pharmacy | NDA020405 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| 1-30 | 31-60 | 61-90 | 91-120 | 121-150 | 151-154 |
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