# Cetrorelix Acetate

NDC: 71288-558
Generic name: Cetrorelix Acetate
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: SUBCUTANEOUS
Marketing started: 20240424

FDA application: ANDA214540

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-558"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-558
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9b3057ac-6cac-4509-a355-df76247b992c