NDC 51991-823 – Everolimus

Everolimus 7.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51991-823

Product details

Brand name
Everolimus
Generic name
Everolimus
Labeler
Breckenridge Pharmaceutical, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205426
Marketed since
March 5, 2021
Listing expires
December 31, 2026
Pharmacologic class
Kinase Inhibitor; mTOR Inhibitor Immunosuppressant

Active ingredients

Uses, dosage, side effects and warnings for Everolimus →

Package NDC codes (2)

Package NDCDescriptionSince
51991-823-284 BLISTER PACK in 1 CARTON (51991-823-28) / 7 TABLET in 1 BLISTER PACK (51991-823-99)Mar 5, 2021
51991-823-3330 TABLET in 1 BOTTLE (51991-823-33)Jun 5, 2023

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