# Fulvestrant

NDC: 71731-6121
Generic name: fulvestrant
Labeler / Manufacturer: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR
Marketing started: 20210401

FDA application: ANDA211422

## Active ingredients

- FULVESTRANT: 50 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71731-6121"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71731-6121
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=46086fe7-190d-4963-97bc-1fe22d36e6d2