United States · FDA National Drug Code directory
PLERIXAFOR
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
- 70710-1208_6eded16b-f43d-4984-bd7c-33ca6d5e3195
- Product NDC
- 70710-1208
- Form
- INJECTION
- Composition / generic term
- plerixafor
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230728
- Source listing expiry
- 20261231
Source-listed ingredients
- PLERIXAFOR — 24 mg/1.2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-USE in 1 CARTON (70710-1208-1) / 1.2 mL in 1 VIAL, SINGLE-USE · 70710-1208-1
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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