United States · FDA National Drug Code directory
Irinotecan hydrochloride
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
- 16714-131_7d7ed052-95ae-6d58-f41f-ada9f8f97b81
- Product NDC
- 16714-131
- Form
- INJECTION
- Composition / generic term
- Irinotecan hydrochloride
- Labeler
- Northstar Rx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201115
- Source listing expiry
- 20261231
Source-listed ingredients
- IRINOTECAN HYDROCHLORIDE — 20 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-DOSE in 1 CARTON (16714-131-01) / 5 mL in 1 VIAL, SINGLE-DOSE · 16714-131-01
Source and coverage
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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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