FDA Application
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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 | 67457-436-50 | Mylan Institutional LLC | ANDA200170 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 62756-826-40 | Sun Pharmaceutical Industries, Inc. | ANDA091418 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0143-9372-01 | Hikma Pharmaceuticals USA Inc. | ANDA064097 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0338-9581-01 | Baxter Healthcare Corporation | HUMAN PRESCRIPTION DRUG | Unapproved drug for use in drug shortage | |
| DOXORUBICIN HYDROCHLORIDE | 43598-541-25 | Dr. Reddy's Laboratories Inc | ANDA208657 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 72603-103-01 | NorthStar RxLLC | ANDA203263 | 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 | 68001-493-26 | BluePoint Laboratories | ANDA203263 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 25021-207-25 | Sagent Pharmaceuticals | ANDA209825 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0069-3033-20 | Pfizer Laboratories Div Pfizer Inc | NDA050629 | HUMAN PRESCRIPTION DRUG | NDA |
| DOXORUBICIN HYDROCHLORIDE | 47335-049-40 | Sun Pharmaceutical Industries, Inc. | ANDA203263 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 70860-208-51 | Athenex Pharmaceutical Division, LLC. | ANDA209825 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 68083-250-01 | Gland Pharma Limited | ANDA209825 | HUMAN PRESCRIPTION DRUG | ANDA |
| DOXORUBICIN HYDROCHLORIDE | 0338-0086-01 | Baxter Healthcare Corporation | NDA050718 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DOXORUBICIN HYDROCHLORIDE | 47335-050-40 | Sun Pharmaceutical Industries, Inc. | ANDA203263 | 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 |
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