NDC 70377-092 – Everolimus

Everolimus 5 mg/1 · Tablet, For Suspension · Oral

Human Prescription Drug

Product NDC70377-092

Product details

Brand name
Everolimus
Generic name
Everolimus
Labeler
Biocon Pharma Inc.
Dosage form
Tablet, For Suspension
Route
Oral
Marketing category
ANDA · ANDA217216
Marketed since
January 14, 2026
Listing expires
December 31, 2027
Pharmacologic class
Kinase Inhibitor; mTOR Inhibitor Immunosuppressant

Active ingredients

Uses, dosage, side effects and warnings for Everolimus →

Package NDC codes (2)

Package NDCDescriptionSince
70377-092-1128 TABLET, FOR SUSPENSION in 1 BOTTLE (70377-092-11)Jan 14, 2026
70377-092-234 BLISTER PACK in 1 CARTON (70377-092-23) / 7 TABLET, FOR SUSPENSION in 1 BLISTER PACKJan 14, 2026

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