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
- 0555-0572_9c7cf5a6-e720-4e83-bb08-f371e9bb9c9e
- Product NDC
- 0555-0572
- Form
- TABLET
- Composition / generic term
- Methotrexate
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19901101
- Source listing expiry
- 20271231
Source-listed ingredients
- METHOTREXATE SODIUM — 2.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0555-0572-02) · 0555-0572-02
- 36 TABLET in 1 BOTTLE (0555-0572-35) · 0555-0572-35
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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