NDC 63323-883 – Doxorubicin Hydrochloride
Doxorubicin Hydrochloride 2 mg/mL · Injection, Solution · Intravenous
Product NDC63323-883
Product details
- Brand name
- Doxorubicin Hydrochloride
- Generic name
- Doxorubicin Hydrochloride
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA063277
- Marketed since
- April 14, 2000
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anthracycline Topoisomerase Inhibitor
Active ingredients
- Doxorubicin Hydrochloride 2 mg/mL
Uses, dosage, side effects and warnings for Doxorubicin Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 63323-883-05 | 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-883-05) / 5 mL in 1 VIAL, SINGLE-DOSE | Apr 14, 2000 |
| 63323-883-10 | 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-883-10) / 10 mL in 1 VIAL, SINGLE-DOSE | Apr 14, 2000 |
| 63323-883-30 | 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-883-30) / 25 mL in 1 VIAL, SINGLE-DOSE | Apr 14, 2000 |
Recalls mentioning this NDC
- D-0105-2021 Dec 2, 2020 · Class III
Cross Contamination with Other Products: trace amounts of octreotide found during testing
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