NDC 61703-408 – Methotrexate
Methotrexate Sodium 25 mg/mL · Injection, Solution · Intramuscular, Intrathecal, Intravenous, Subcutaneous
Product NDC61703-408
Product details
- Brand name
- Methotrexate
- Generic name
- Methotrexate
- Labeler
- Hospira, Inc.
- Dosage form
- Injection, Solution
- Route
- Intramuscular, Intrathecal, Intravenous, Subcutaneous
- Marketing category
- NDA · NDA011719
- Marketed since
- November 11, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Folate Analog Metabolic Inhibitor
Active ingredients
- Methotrexate Sodium 25 mg/mL
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 61703-408-25 | 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-408-25) / 40 mL in 1 VIAL, SINGLE-DOSE | Nov 11, 2013 |
| 61703-408-41 | 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-408-41) / 40 mL in 1 VIAL, SINGLE-DOSE | Feb 26, 2001 |
Recalls mentioning this NDC
- D-0553-2021 Jun 2, 2021 · Class II
CGMP Deviations: Intermittent exposure to temperature excursion during storage. - D-1681-2012 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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