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 | 0338-9581-02 | Baxter Healthcare Corporation | HUMAN PRESCRIPTION DRUG | Unapproved drug for use in drug shortage | |
| DOXORUBICIN HYDROCHLORIDE | 0338-9581-01 | Baxter Healthcare Corporation | HUMAN PRESCRIPTION DRUG | Unapproved drug for use in drug shortage | |
| DOXORUBICIN HYDROCHLORIDE | 0143-9092-01 | 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 | 0143-9093-01 | 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 | 0143-9548-10 | 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 | 0143-9371-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9084-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9549-10 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9369-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9547-01 | 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 | 0143-9370-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9549-01 | 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 | 0143-9086-01 | Hikma Pharmaceuticals USA Inc. | ANDA062975 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9088-01 | 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 | 63323-101-61 | Fresenius Kabi USA, LLC | ANDA063277 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 63323-883-10 | Fresenius Kabi USA, LLC | ANDA063277 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 63323-883-05 | Fresenius Kabi USA, LLC | ANDA063277 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 63323-883-30 | Fresenius Kabi USA, LLC | ANDA063277 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9546-01 | Hikma Pharmaceuticals USA Inc. | ANDA064097 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9087-01 | Hikma Pharmaceuticals USA Inc. | ANDA064097 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9091-01 | Hikma Pharmaceuticals USA Inc. | ANDA064097 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9372-01 | Hikma Pharmaceuticals USA Inc. | ANDA064097 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 62756-826-40 | Sun Pharmaceutical Industries, Inc. | ANDA091418 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 62756-827-40 | Sun Pharmaceutical Industries, Inc. | ANDA091418 | HUMAN PRESCRIPTION DRUG | ANDA |
| 1-30 | 31-60 | 61-78 |
-
