NDC 87628-101 – Varubi

Rolapitant Hydrochloride 90 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC87628-101

Product details

Brand name
Varubi
Generic name
Rolapitant
Labeler
Luria Therapeutics LLC
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA206500
Marketed since
August 20, 2026
Listing expires
December 31, 2027
Pharmacologic class
Substance P/Neurokinin-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Varubi →

Package NDC codes (1)

Package NDCDescriptionSince
87628-101-022 TABLET in 1 BLISTER PACK (87628-101-02)Sep 8, 2026

Other Varubi products