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
68071-3765_2bae0372-8ccb-0028-e063-6294a90a889f
Product NDC
68071-3765
Form
TABLET
Composition / generic term
Methotrexate
Labeler
NuCare Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20200130
Source listing expiry
20261231

Source-listed ingredients

  • METHOTREXATE SODIUM — 2.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET in 1 BOTTLE (68071-3765-6) · 68071-3765-6
  • 90 TABLET in 1 BOTTLE (68071-3765-9) · 68071-3765-9

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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