Package 31722-083-05

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-083-05
Digits Only 3172208305
Product NDC 31722-083
Product ID 31722-083_3a429e3e-35e3-c6bb-e063-6294a90ac9ee
Description

500 TABLET, FILM COATED in 1 BOTTLE (31722-083-05)

Marketing

Marketing Status
Marketed Since 2024-08-21
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": "3a429e3e-35e3-c6bb-e063-6294a90ac9ee", "openfda": {"upc": ["0331722083300"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["c80625bb-7857-4763-81fe-542b3448d84f"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-083-05)", "package_ndc": "31722-083-05", "marketing_start_date": "20240821"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-083-30)", "package_ndc": "31722-083-30", "marketing_start_date": "20240821"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-083-90)", "package_ndc": "31722-083-90", "marketing_start_date": "20240821"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "31722-083_3a429e3e-35e3-c6bb-e063-6294a90ac9ee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "31722-083", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA218174", "marketing_category": "ANDA", "marketing_start_date": "20240821", "listing_expiration_date": "20261231"}