NDC 0781-2323 – Aprepitant

Aprepitant 125 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC0781-2323

Product details

Brand name
Aprepitant
Generic name
Aprepitant
Labeler
Sandoz Inc
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA090999
Marketed since
December 27, 2016
Listing expires
December 31, 2026
Pharmacologic class
Substance P/Neurokinin-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Aprepitant →

Package NDC codes (1)

Package NDCDescriptionSince
0781-2323-681 BLISTER PACK in 1 CARTON (0781-2323-68) / 6 CAPSULE in 1 BLISTER PACK (0781-2323-06)Dec 27, 2016

Recalls mentioning this NDC

Other Aprepitant products