Package 43598-355-30

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43598-355-30
Digits Only 4359835530
Product NDC 43598-355
Product ID 43598-355_a6742369-fc8f-d7cc-42c1-33c95d6946ef
Description

30 TABLET, FILM COATED in 1 BOTTLE (43598-355-30)

Marketing

Marketing Status
Marketed Since 2023-02-20
Brand lurasidone hydrochloride
Generic lurasidone hydrochloride
Sample Package No

Linked Drug Pages (1)

Lurasidone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a6742369-fc8f-d7cc-42c1-33c95d6946ef", "openfda": {"upc": ["0343598355306"], "unii": ["O0P4I5851I"], "rxcui": ["1297278"], "spl_set_id": ["2f22a0bd-94f3-53d7-717c-03da8e1a7e97"], "manufacturer_name": ["Dr. Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (43598-355-30)", "package_ndc": "43598-355-30", "marketing_start_date": "20230220"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "43598-355_a6742369-fc8f-d7cc-42c1-33c95d6946ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "43598-355", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Dr. Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA208055", "marketing_category": "ANDA", "marketing_start_date": "20230220", "listing_expiration_date": "20261231"}