Package 72162-2209-3

Brand: tamoxifen citrate

Generic: tamoxifen citrate
NDC Package

Package Facts

Identity

Package NDC 72162-2209-3
Digits Only 7216222093
Product NDC 72162-2209
Product ID 72162-2209_8222e567-8174-40fc-afd8-ab6bde6dc073
Description

30 TABLET, FILM COATED in 1 BOTTLE (72162-2209-3)

Marketing

Marketing Status
Marketed Since 2024-01-05
Brand tamoxifen citrate
Generic tamoxifen citrate
Sample Package No

Linked Drug Pages (1)

Tamoxifen Citrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8222e567-8174-40fc-afd8-ab6bde6dc073", "openfda": {"unii": ["7FRV7310N6"], "rxcui": ["313195"], "spl_set_id": ["9b4a8abc-6e56-40c5-a826-1d1f3c0786e1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-2209-3)", "package_ndc": "72162-2209-3", "marketing_start_date": "20240105"}], "brand_name": "Tamoxifen Citrate", "product_id": "72162-2209_8222e567-8174-40fc-afd8-ab6bde6dc073", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "72162-2209", "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": "20 mg/1"}], "application_number": "ANDA213358", "marketing_category": "ANDA", "marketing_start_date": "20200814", "listing_expiration_date": "20261231"}