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
- 70121-1222_350853a3-6178-4d83-b5c4-75b3e4c1799d
- Product NDC
- 70121-1222
- Form
- INJECTION
- Composition / generic term
- Docetaxel
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180119
- Source listing expiry
- 20261231
Source-listed ingredients
- DOCETAXEL ANHYDROUS — 80 mg/4mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, GLASS in 1 CARTON (70121-1222-1) / 4 mL in 1 VIAL, GLASS · 70121-1222-1
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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