United States · FDA National Drug Code directory
Docetaxel
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
- 43598-611_948f7c4c-6a40-d240-3eb3-d9ae6e371429
- Product NDC
- 43598-611
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Docetaxel
- Labeler
- Dr. Reddy's Laboratories Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170822
- Source listing expiry
- 20261231
Source-listed ingredients
- DOCETAXEL — 20 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 mL in 1 VIAL, GLASS (43598-611-11) · 43598-611-11
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.
Browse United States records →