United States · FDA National Drug Code directory

Everolimus

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
49884-160_bf8637b9-79c5-42fc-8de0-b6209ad745f0
Product NDC
49884-160
Form
TABLET
Composition / generic term
Everolimus
Labeler
Par Health USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20221216
Source listing expiry
20261231

Source-listed ingredients

  • EVEROLIMUS — .75 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 6 BLISTER PACK in 1 CARTON (49884-160-02) / 10 TABLET in 1 BLISTER PACK (49884-160-52) · 49884-160-02

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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