NDC 47335-892 – Temozolomide

Temozolomide 100 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC47335-892

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
47335-892-211 BOTTLE in 1 CARTON (47335-892-21) / 14 CAPSULE in 1 BOTTLEFeb 13, 2014
47335-892-7215 BLISTER PACK in 1 CARTON (47335-892-72) / 1 CAPSULE in 1 BLISTER PACKFeb 13, 2014
47335-892-745 BLISTER PACK in 1 CARTON (47335-892-74) / 1 CAPSULE in 1 BLISTER PACKFeb 13, 2014
47335-892-7520 BLISTER PACK in 1 CARTON (47335-892-75) / 1 CAPSULE in 1 BLISTER PACKFeb 13, 2014
47335-892-801 BOTTLE in 1 CARTON (47335-892-80) / 5 CAPSULE in 1 BOTTLEFeb 13, 2014
47335-892-871 BOTTLE in 1 CARTON (47335-892-87) / 20 CAPSULE in 1 BOTTLEFeb 13, 2014

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