NDC 68462-583 – Aprepitant

Aprepitant 40 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC68462-583

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 (3)

Package NDCDescriptionSince
68462-583-111 BLISTER PACK in 1 CARTON (68462-583-11) / 10 CAPSULE in 1 BLISTER PACKOct 12, 2017
68462-583-401 BLISTER PACK in 1 CARTON (68462-583-40) / 1 CAPSULE in 1 BLISTER PACKOct 12, 2017
68462-583-855 BLISTER PACK in 1 CARTON (68462-583-85) / 1 CAPSULE in 1 BLISTER PACKOct 12, 2017

Recalls mentioning this NDC

Other Aprepitant products