NDC 68462-585 – Aprepitant

Aprepitant 125 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC68462-585

Product details

Brand name
Aprepitant
Generic name
Aprepitant
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207777
Marketed since
October 12, 2017
Listing expires
December 31, 2027
Pharmacologic class
Substance P/Neurokinin-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Aprepitant →

Package NDC codes (1)

Package NDCDescriptionSince
68462-585-761 BLISTER PACK in 1 CARTON (68462-585-76) / 6 CAPSULE in 1 BLISTER PACK (68462-585-40)Oct 12, 2017

Recalls mentioning this NDC

Other Aprepitant products