United States · FDA National Drug Code directory
Fulvestrant
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
- 71288-555_2be67b09-31de-41b4-9468-a73a284abe41
- Product NDC
- 71288-555
- Form
- INJECTION
- Composition / generic term
- Fulvestrant
- Labeler
- Meitheal Pharmaceuticals Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191121 / 20270131
Source-listed ingredients
- FULVESTRANT — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 SYRINGE in 1 CARTON (71288-555-86) / 5 mL in 1 SYRINGE (71288-555-85) · 71288-555-86
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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