FDA Application
-
NDC Search Results on Active Ingredient: doxorubicin
Click on Active Ingredient to view the label.
| Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
|---|---|---|---|---|---|
| DOXORUBICIN HYDROCHLORIDE | 0069-3030-20 | Pfizer Laboratories Div Pfizer Inc | NDA050629 | HUMAN PRESCRIPTION DRUG | NDA |
| DOXORUBICIN HYDROCHLORIDE | 0069-3031-20 | Pfizer Laboratories Div Pfizer Inc | NDA050629 | HUMAN PRESCRIPTION DRUG | NDA |
| DOXORUBICIN HYDROCHLORIDE | 0069-3032-20 | Pfizer Laboratories Div Pfizer Inc | NDA050629 | HUMAN PRESCRIPTION DRUG | NDA |
| DOXORUBICIN HYDROCHLORIDE | 0069-3033-20 | Pfizer Laboratories Div Pfizer Inc | NDA050629 | HUMAN PRESCRIPTION DRUG | NDA |
| DOXORUBICIN HYDROCHLORIDE | 0069-3034-20 | Pfizer Laboratories Div Pfizer Inc | NDA050629 | HUMAN PRESCRIPTION DRUG | NDA |
| DOXORUBICIN HYDROCHLORIDE | 0069-4004-05 | Pfizer Laboratories Div Pfizer Inc | NDA050629 | HUMAN PRESCRIPTION DRUG | NDA |
| DOXORUBICIN HYDROCHLORIDE | 0069-4015-10 | Pfizer Laboratories Div Pfizer Inc | NDA050629 | HUMAN PRESCRIPTION DRUG | NDA |
| DOXORUBICIN HYDROCHLORIDE | 0069-4026-25 | Pfizer Laboratories Div Pfizer Inc | NDA050629 | HUMAN PRESCRIPTION DRUG | NDA |
| DOXORUBICIN HYDROCHLORIDE | 0069-4037-01 | Pfizer Laboratories Div Pfizer Inc | NDA050629 | HUMAN PRESCRIPTION DRUG | NDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9084-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9085-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9086-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9087-01 | Hikma Pharmaceuticals USA Inc. | ANDA064097 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9088-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9089-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9090-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9091-01 | Hikma Pharmaceuticals USA Inc. | ANDA064097 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9092-01 | Hikma Pharmaceuticals USA Inc. | ANDA062921 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9093-01 | Hikma Pharmaceuticals USA Inc. | ANDA062921 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9275-01 | Hikma Pharmaceuticals USA Inc. | ANDA062921 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9277-01 | Hikma Pharmaceuticals USA Inc. | ANDA062921 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9369-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9370-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9371-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9372-01 | Hikma Pharmaceuticals USA Inc. | ANDA064097 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9546-01 | Hikma Pharmaceuticals USA Inc. | ANDA064097 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9547-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9548-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9548-10 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9549-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| 1-30 | 31-60 | 61-78 |
-
