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
16729-436_3001d1ed-b200-7d1b-e063-6394a90ab45f
Product NDC
16729-436
Form
INJECTION
Composition / generic term
Fulvestrant
Labeler
Accord Healthcare Inc.
Marketing category
ANDA
Marketing start / end (source format)
20210121
Source listing expiry
20261231

Source-listed ingredients

  • FULVESTRANT — 250 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 SYRINGE, GLASS in 1 CARTON (16729-436-30) / 5 mL in 1 SYRINGE, GLASS (16729-436-31) · 16729-436-30

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 →