United States · FDA National Drug Code directory

CISPLATIN

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
68001-608_0c3ef530-de61-73f7-e063-6294a90a9973
Product NDC
68001-608
Form
INJECTION, SOLUTION
Composition / generic term
Cisplatin
Labeler
BluePoint Laboratories
Marketing category
ANDA
Marketing start / end (source format)
20240101
Source listing expiry
20261231

Source-listed ingredients

  • CISPLATIN — 1 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL in 1 CARTON (68001-608-24) / 50 mL in 1 VIAL · 68001-608-24

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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