NDC 0781-4063 – Aprepitant

· Kit

Human Prescription Drug 1 recall

Product NDC0781-4063

Product details

Brand name
Aprepitant
Generic name
Aprepitant
Labeler
Sandoz Inc
Dosage form
Kit
Marketing category
ANDA · ANDA090999
Marketed since
December 27, 2016
Listing expires
December 31, 2026

Active ingredients

    Uses, dosage, side effects and warnings for Aprepitant →

    Package NDC codes (1)

    Package NDCDescriptionSince
    0781-4063-361 KIT in 1 DOSE PACK (0781-4063-36) * 1 CAPSULE in 1 BLISTER PACK * 2 CAPSULE in 1 BLISTER PACKDec 27, 2016

    Recalls mentioning this NDC

    Other Aprepitant products