NDC 68462-112 – Aprepitant

· Kit

Human Prescription Drug 1 recall

Product NDC68462-112

Product details

Brand name
Aprepitant
Generic name
Aprepitant
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Kit
Marketing category
ANDA · ANDA207777
Marketed since
October 12, 2017
Listing expires
December 31, 2027

Active ingredients

    Uses, dosage, side effects and warnings for Aprepitant →

    Package NDC codes (1)

    Package NDCDescriptionSince
    68462-112-331 KIT in 1 DOSE PACK (68462-112-33) * 2 CAPSULE in 1 BLISTER PACK * 1 CAPSULE in 1 BLISTER PACKOct 12, 2017

    Recalls mentioning this NDC

    Other Aprepitant products