NDC 47335-891 – Temozolomide

Temozolomide 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC47335-891

Product details

Brand name
Temozolomide
Generic name
Temozolomide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA201742
Marketed since
February 13, 2014
Listing expires
December 31, 2026
Pharmacologic class
Alkylating Drug

Active ingredients

Uses, dosage, side effects and warnings for Temozolomide →

Package NDC codes (6)

Package NDCDescriptionSince
47335-891-211 BOTTLE in 1 CARTON (47335-891-21) / 14 CAPSULE in 1 BOTTLEFeb 13, 2014
47335-891-7215 BLISTER PACK in 1 CARTON (47335-891-72) / 1 CAPSULE in 1 BLISTER PACKFeb 13, 2014
47335-891-745 BLISTER PACK in 1 CARTON (47335-891-74) / 1 CAPSULE in 1 BLISTER PACKFeb 13, 2014
47335-891-7520 BLISTER PACK in 1 CARTON (47335-891-75) / 1 CAPSULE in 1 BLISTER PACKFeb 13, 2014
47335-891-801 BOTTLE in 1 CARTON (47335-891-80) / 5 CAPSULE in 1 BOTTLEFeb 13, 2014
47335-891-871 BOTTLE in 1 CARTON (47335-891-87) / 20 CAPSULE in 1 BOTTLEFeb 13, 2014

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