DOXORUBICIN HYDROCHLORIDE
DOXORUBICIN HYDROCHLORIDE
INTRAVENOUS
HUMAN PRESCRIPTION DRUG
DOXORUBICIN HYDROCHLORIDE is an FDA drug label for the active ingredient DOXORUBICIN HYDROCHLORIDE manufactured by Zydus Lifesciences Limited administered by INTRAVENOUS. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20221101.
- Generic name
- DOXORUBICIN HYDROCHLORIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- INTRAVENOUS
- Dosage form
- N/A
- NDC
- 49315-008
- Application
- ANDA212299
- Label effective
- 20221101
Indications & Usage
Not available.
Dosage & Administration
Not available.
Contraindications
Not available.
Warnings
Not available.
Adverse Reactions
Not available.