Package 53746-880-30

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53746-880-30
Digits Only 5374688030
Product NDC 53746-880
Product ID 53746-880_f81d4ba1-6578-46ad-bbc6-7c80a6e37625
Description

30 TABLET, COATED in 1 BOTTLE (53746-880-30)

Marketing

Marketing Status
Marketed Since 2024-07-05
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": "f81d4ba1-6578-46ad-bbc6-7c80a6e37625", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["84648adf-b3c6-476e-8d11-2a9d7c5eb550"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (53746-880-30)", "package_ndc": "53746-880-30", "marketing_start_date": "20240705"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "53746-880_f81d4ba1-6578-46ad-bbc6-7c80a6e37625", "dosage_form": "TABLET, COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "53746-880", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208002", "marketing_category": "ANDA", "marketing_start_date": "20240705", "listing_expiration_date": "20261231"}