United States · FDA National Drug Code directory
Ganirelix Acetate
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
- 67184-0574_edcb57c8-5b08-4076-b67c-93d6d610525d
- Product NDC
- 67184-0574
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Ganirelix Acetate
- Labeler
- Qilu Pharmaceutical Co., Ltd.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250515
- 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 (67184-0574-1) / 1 SYRINGE, GLASS in 1 BLISTER PACK / 1 mL in 1 SYRINGE, GLASS · 67184-0574-1
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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