NDC 0703-3675 – Methotrexate
Methotrexate Sodium 25 mg/mL · Injection, Solution · Intra-arterial, Intramuscular, Intrathecal, Intravenous
Product NDC0703-3675
Product details
- Brand name
- Methotrexate
- Generic name
- Methotrexate
- Labeler
- Teva Parenteral Medicines, Inc.
- Dosage form
- Injection, Solution
- Route
- Intra-arterial, Intramuscular, Intrathecal, Intravenous
- Marketing category
- ANDA · ANDA040843
- Marketed since
- August 1, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Folate Analog Metabolic Inhibitor
Active ingredients
- Methotrexate Sodium 25 mg/mL
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0703-3675-01 | 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3675-01) / 10 mL in 1 VIAL, SINGLE-DOSE | Aug 1, 2012 |
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