lurasidone hydrochloride

Generic: lurasidone hydrochloride

Labeler: golden state medical supply, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lurasidone hydrochloride
Generic Name lurasidone hydrochloride
Labeler golden state medical supply, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

lurasidone hydrochloride 40 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 51407-832
Product ID 51407-832_4655e19e-554d-0a05-e063-6294a90ab7a9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208058
Marketing Start 2019-09-04
Marketing End 2026-09-30

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51407832
Hyphenated Format 51407-832

Supplemental Identifiers

RxCUI
1040031 1040041
UNII
O0P4I5851I

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lurasidone hydrochloride (source: ndc)
Generic Name lurasidone hydrochloride (source: ndc)
Application Number ANDA208058 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (51407-832-05)
source: ndc

Packages (1)

51407-832-05 500 TABLET, FILM COATED in 1 BOTTLE (51407-832-05)

Ingredients (1)

lurasidone hydrochloride (40 mg/1)

Linked Drug Pages (1)

Lurasidone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4655e19e-554d-0a05-e063-6294a90ab7a9", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041"], "spl_set_id": ["08ba1a4c-c193-e0ea-e063-6294a90a52dc"], "manufacturer_name": ["Golden State Medical Supply, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (51407-832-05)", "package_ndc": "51407-832-05", "marketing_end_date": "20260930", "marketing_start_date": "20231023"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "51407-832_4655e19e-554d-0a05-e063-6294a90ab7a9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "51407-832", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208058", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20190904"}