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
- 67877-718_33247fe5-9b47-4513-93fe-fc65e4c1b63f
- Product NDC
- 67877-718
- Form
- TABLET
- Composition / generic term
- Everolimus
- Labeler
- Ascend Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211127
- Source listing expiry
- 20261231
Source-listed ingredients
- EVEROLIMUS — .25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 BLISTER PACK in 1 CARTON (67877-718-31) / 10 TABLET in 1 BLISTER PACK (67877-718-33) · 67877-718-31
- 60 TABLET in 1 BOTTLE (67877-718-60) · 67877-718-60
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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