Package 69097-938-02

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69097-938-02
Digits Only 6909793802
Product NDC 69097-938
Product ID 69097-938_38789037-ee81-405e-85fc-a4cf40760a3e
Description

30 TABLET, FILM COATED in 1 BOTTLE (69097-938-02)

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": "38789037-ee81-405e-85fc-a4cf40760a3e", "openfda": {"upc": ["0369097939021", "0369097937027", "0369097942021"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["76c055aa-d96a-42e5-a670-1db63b9c1dd6"], "manufacturer_name": ["Cipla USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69097-938-02)", "package_ndc": "69097-938-02", "marketing_start_date": "20230220"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "69097-938_38789037-ee81-405e-85fc-a4cf40760a3e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "69097-938", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Cipla USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA208028", "marketing_category": "ANDA", "marketing_start_date": "20230220", "listing_expiration_date": "20261231"}