United States · FDA National Drug Code directory
Methotrexate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 61703-161_6bb8643f-6ab4-4e1c-bcf9-b82e8cf18910
- Product NDC
- 61703-161
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Methotrexate
- Labeler
- Hospira, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20241104
- Source listing expiry
- 20261231
Source-listed ingredients
- METHOTREXATE SODIUM — 25 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 VIAL, MULTI-DOSE in 1 CARTON (61703-161-05) / 2 mL in 1 VIAL, MULTI-DOSE (61703-161-02) · 61703-161-05
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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