# Tamoxifen Citrate

NDC: 68071-3990
Generic name: Tamoxifen Citrate
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
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

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-3990"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3990
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=509f8ba3-214d-aec8-e063-6294a90af498