NDC 82293-032 – Everolimus

Everolimus 7.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82293-032

Product details

Brand name
Everolimus
Generic name
Everolimus
Labeler
Novugen Pharma (USA) LLC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA219955
Marketed since
March 30, 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 (3)

Package NDCDescriptionSince
82293-032-1028 TABLET in 1 BOTTLE (82293-032-10)Mar 30, 2026
82293-032-214 BLISTER PACK in 1 CARTON (82293-032-21) / 7 TABLET in 1 BLISTER PACK (82293-032-20)Mar 30, 2026
82293-032-311 POUCH in 1 CARTON (82293-032-31) / 3 BLISTER PACK in 1 POUCH / 10 TABLET in 1 BLISTER PACK (82293-032-30)Mar 30, 2026

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