NDC 47335-929 – Temozolomide

Temozolomide 140 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC47335-929

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
47335-929-211 BOTTLE in 1 CARTON (47335-929-21) / 14 CAPSULE in 1 BOTTLEFeb 13, 2014
47335-929-7215 BLISTER PACK in 1 CARTON (47335-929-72) / 1 CAPSULE in 1 BLISTER PACKFeb 13, 2014
47335-929-745 BLISTER PACK in 1 CARTON (47335-929-74) / 1 CAPSULE in 1 BLISTER PACKFeb 13, 2014
47335-929-7520 BLISTER PACK in 1 CARTON (47335-929-75) / 1 CAPSULE in 1 BLISTER PACKFeb 13, 2014
47335-929-801 BOTTLE in 1 CARTON (47335-929-80) / 5 CAPSULE in 1 BOTTLEFeb 13, 2014
47335-929-871 BOTTLE in 1 CARTON (47335-929-87) / 20 CAPSULE in 1 BOTTLEFeb 13, 2014

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