United States · FDA National Drug Code directory

JAYTHARI

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
70710-1749_1dafee9d-1cc2-41a8-bc75-10cea25fcd0f
Product NDC
70710-1749
Form
TABLET
Composition / generic term
Deflazacort
Labeler
Zydus Pharmaceuticals (USA) Inc.
Marketing category
ANDA
Marketing start / end (source format)
20250612
Source listing expiry
20271231

Source-listed ingredients

  • DEFLAZACORT — 6 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (70710-1749-1) / 100 TABLET in 1 BOTTLE · 70710-1749-1

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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