United States · FDA National Drug Code directory

Leucovorin Calcium

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
68001-417_d5ee26ca-d963-687f-e053-2a95a90a2a50
Product NDC
68001-417
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
Leucovorin Calcium
Labeler
BluePoint Laboratories
Marketing category
ANDA
Marketing start / end (source format)
20190926
Source listing expiry
20261231

Source-listed ingredients

  • LEUCOVORIN CALCIUM — 200 mg/20mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL in 1 BOX, UNIT-DOSE (68001-417-37) / 20 mL in 1 VIAL · 68001-417-37

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →