Package 59651-300-90

Brand: tamoxifen citrate

Generic: tamoxifen citrate
NDC Package

Package Facts

Identity

Package NDC 59651-300-90
Digits Only 5965130090
Product NDC 59651-300
Description

90 TABLET, FILM COATED in 1 BOTTLE (59651-300-90)

Marketing

Marketing Status
Marketed Since 2020-08-14
Brand tamoxifen citrate
Generic tamoxifen citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a596c715-8e30-43c1-aba3-4fe5de6729fa", "openfda": {"unii": ["7FRV7310N6"], "rxcui": ["198240", "313195"], "spl_set_id": ["a596c715-8e30-43c1-aba3-4fe5de6729fa"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (59651-300-30)", "package_ndc": "59651-300-30", "marketing_start_date": "20200814"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (59651-300-90)", "package_ndc": "59651-300-90", "marketing_start_date": "20200814"}], "brand_name": "Tamoxifen Citrate", "product_id": "59651-300_a596c715-8e30-43c1-aba3-4fe5de6729fa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "59651-300", "generic_name": "Tamoxifen Citrate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamoxifen Citrate", "active_ingredients": [{"name": "TAMOXIFEN CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA213358", "marketing_category": "ANDA", "marketing_start_date": "20200814", "listing_expiration_date": "20261231"}