NDC 0703-5747 – Cisplatin

Cisplatin 50 mg/50mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC0703-5747

Product details

Brand name
Cisplatin
Generic name
Cisplatin
Labeler
Teva Parenteral Medicines, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA074656
Marketed since
June 1, 2000
Listing expires
December 31, 2026
Pharmacologic class
Platinum-based Drug

Active ingredients

Uses, dosage, side effects and warnings for Cisplatin →

Package NDC codes (1)

Package NDCDescriptionSince
0703-5747-111 VIAL, MULTI-DOSE in 1 CARTON (0703-5747-11) / 50 mL in 1 VIAL, MULTI-DOSEJun 1, 2000

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