NDC 13668-711 – Nilotinib

Nilotinib Hydrochloride Monohydrate 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC13668-711

Product details

Brand name
Nilotinib
Generic name
Nilotinib
Labeler
Torrent Pharmaceuticals Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA218532
Marketed since
December 16, 2025
Listing expires
December 31, 2027
Pharmacologic class
Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Nilotinib →

Package NDC codes (2)

Package NDCDescriptionSince
13668-711-574 BLISTER PACK in 1 CARTON (13668-711-57) / 28 CAPSULE in 1 BLISTER PACKDec 16, 2025
13668-711-911 BLISTER PACK in 1 CARTON (13668-711-91) / 28 CAPSULE in 1 BLISTER PACKDec 16, 2025

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