Package 72189-415-30

Brand: anastrozole

Generic: anastrozole
NDC Package

Package Facts

Identity

Package NDC 72189-415-30
Digits Only 7218941530
Product NDC 72189-415
Description

30 TABLET in 1 BOTTLE (72189-415-30)

Marketing

Marketing Status
Marketed Since 2023-01-30
Brand anastrozole
Generic anastrozole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4d028d-1373-45ab-e063-6394a90a0353", "openfda": {"nui": ["N0000175563", "N0000175080"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["f37db328-bb81-9df9-e053-2a95a90a6f43"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-415-30)", "package_ndc": "72189-415-30", "marketing_start_date": "20230130"}], "brand_name": "ANASTROZOLE", "product_id": "72189-415_2c4d028d-1373-45ab-e063-6394a90a0353", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "72189-415", "generic_name": "ANASTROZOLE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ANASTROZOLE", "active_ingredients": [{"name": "ANASTROZOLE", "strength": "1 mg/1"}], "application_number": "ANDA090568", "marketing_category": "ANDA", "marketing_start_date": "20230130", "listing_expiration_date": "20261231"}