# Tamoxifen Citrate

NDC: 75907-059
Generic name: Tamoxifen Citrate
Labeler / Manufacturer: Dr. Reddy's Labratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240822

FDA application: ANDA075797

## Active ingredients

- TAMOXIFEN CITRATE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"75907-059"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75907-059
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c6c6a643-57d6-7ea5-7da0-e8a66802468a