United States · FDA National Drug Code directory

Azathioprine

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
70518-3544_4f58b212-db57-4132-e063-6394a90a1cdf
Product NDC
70518-3544
Form
TABLET
Composition / generic term
Azathioprine
Labeler
REMEDYREPACK INC.
Marketing category
ANDA
Marketing start / end (source format)
20220930
Source listing expiry
20271231

Source-listed ingredients

  • AZATHIOPRINE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 POUCH in 1 BOX (70518-3544-0) / 1 TABLET in 1 POUCH (70518-3544-1) · 70518-3544-0

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.

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