United States · FDA National Drug Code directory

Fyremadel

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
55566-1010_5b000831-15ef-44ff-9fce-3a2289d5e047
Product NDC
55566-1010
Form
INJECTION, SOLUTION
Composition / generic term
ganirelix acetate
Labeler
Ferring Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20220228
Source listing expiry
20261231

Source-listed ingredients

  • GANIRELIX ACETATE — 250 ug/.5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (55566-1010-1) / 1 SYRINGE in 1 BLISTER PACK / .5 mL in 1 SYRINGE · 55566-1010-1

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.

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