Package 60687-769-94

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-769-94
Digits Only 6068776994
Product NDC 60687-769
Description

20 BLISTER PACK in 1 CARTON (60687-769-94) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-769-11)

Marketing

Marketing Status
Marketed Since 2023-05-09
Brand lurasidone hydrochloride
Generic lurasidone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2abe376d-e980-af98-e063-6394a90ac3ef", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1431235"], "spl_set_id": ["b83e1015-8016-4c7c-8239-8dba3a882e46"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (60687-769-94)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-769-11)", "package_ndc": "60687-769-94", "marketing_start_date": "20230509"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "60687-769_2abe376d-e980-af98-e063-6394a90ac3ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "60687-769", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA212244", "marketing_category": "ANDA", "marketing_start_date": "20230509", "listing_expiration_date": "20261231"}