Doxorubicin Hydrochloride
- Product NDC
- 0143-9090
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxorubicin Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA062975
- Marketing category
- ANDA
- Substance
- DOXORUBICIN HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 0143-9090-01 | 1 VIAL in 1 BOX (0143-9090-01) / 25 mL in 1 VIAL | 2019-10-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Doxorubicin Hydrochloride | Hikma Pharmaceuticals USA Inc. | 2024-01-16 | HUMAN PRESCRIPTION DRUG LABEL | 3 |