# Tamoxifen Citrate

NDC: 59651-299
Generic name: Tamoxifen Citrate
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200814

FDA application: ANDA213358

## Active ingredients

- TAMOXIFEN CITRATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-299"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-299
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a596c715-8e30-43c1-aba3-4fe5de6729fa