Package 72162-2208-6

Brand: tamoxifen citrate

Generic: tamoxifen citrate
NDC Package

Package Facts

Identity

Package NDC 72162-2208-6
Digits Only 7216222086
Product NDC 72162-2208
Description

60 TABLET, FILM COATED in 1 BOTTLE (72162-2208-6)

Marketing

Marketing Status
Marketed Since 2024-01-05
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": "681529be-51fc-4ac3-902a-2e00beb327a9", "openfda": {"unii": ["7FRV7310N6"], "rxcui": ["198240"], "spl_set_id": ["feb96056-79f5-4024-ab0e-fdbb8d4ab862"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72162-2208-6)", "package_ndc": "72162-2208-6", "marketing_start_date": "20240105"}], "brand_name": "Tamoxifen Citrate", "product_id": "72162-2208_681529be-51fc-4ac3-902a-2e00beb327a9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "72162-2208", "generic_name": "Tamoxifen Citrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamoxifen Citrate", "active_ingredients": [{"name": "TAMOXIFEN CITRATE", "strength": "10 mg/1"}], "application_number": "ANDA213358", "marketing_category": "ANDA", "marketing_start_date": "20200814", "listing_expiration_date": "20261231"}