Package 72189-598-30

Brand: lurasidone hcl

Generic: lurasidone hcl
NDC Package

Package Facts

Identity

Package NDC 72189-598-30
Digits Only 7218959830
Product NDC 72189-598
Product ID 72189-598_296811cf-cba9-16c2-e063-6294a90acfa6
Description

30 TABLET in 1 BOTTLE (72189-598-30)

Marketing

Marketing Status
Marketed Since 2024-12-16
Brand lurasidone hcl
Generic lurasidone hcl
Sample Package No

Linked Drug Pages (1)

Lurasidone HCL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "296811cf-cba9-16c2-e063-6294a90acfa6", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031"], "spl_set_id": ["296811cf-cba8-16c2-e063-6294a90acfa6"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-598-30)", "package_ndc": "72189-598-30", "marketing_start_date": "20241216"}], "brand_name": "Lurasidone HCL", "product_id": "72189-598_296811cf-cba9-16c2-e063-6294a90acfa6", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-598", "generic_name": "Lurasidone HCL", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone HCL", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208045", "marketing_category": "ANDA", "marketing_start_date": "20241216", "listing_expiration_date": "20261231"}