NDC 61703-342 – Paclitaxel
Paclitaxel 6 mg/mL · Injection, Solution · Intravenous
Product NDC61703-342
Product details
- Brand name
- Paclitaxel
- Generic name
- Paclitaxel
- Labeler
- Hospira, Inc.
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA076131
- Marketed since
- March 1, 2004
- Listing expires
- December 31, 2027
- Pharmacologic class
- Microtubule Inhibitor
Active ingredients
- Paclitaxel 6 mg/mL
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 61703-342-09 | 1 VIAL, MULTI-DOSE in 1 CARTON (61703-342-09) / 5 mL in 1 VIAL, MULTI-DOSE | Mar 1, 2004 |
| 61703-342-22 | 1 VIAL, MULTI-DOSE in 1 CARTON (61703-342-22) / 16.7 mL in 1 VIAL, MULTI-DOSE | Mar 1, 2004 |
| 61703-342-50 | 1 VIAL, MULTI-DOSE in 1 CARTON (61703-342-50) / 50 mL in 1 VIAL, MULTI-DOSE | Mar 1, 2004 |
Recalls mentioning this NDC
- D-1682-2012 Sep 26, 2012 · Class II
The affected lots of Carboplatin Injection, Cytarabine Injection, Methotrexate Injection, USP, and Paclitaxel Injection are being recalled due to visible particles embedded in the glass located at…
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