lurasidone hydrochloride

Generic: lurasidone hydrochloride

Labeler: alembic pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lurasidone hydrochloride
Generic Name lurasidone hydrochloride
Labeler alembic pharmaceuticals limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

lurasidone hydrochloride 40 mg/1

Manufacturer
Alembic Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 46708-495
Product ID 46708-495_a4f0715d-590f-4b13-bb72-19cdca95aa01
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213248
Listing Expiration 2026-12-31
Marketing Start 2023-01-24

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46708495
Hyphenated Format 46708-495

Supplemental Identifiers

RxCUI
1040031 1040041 1235247 1297278 1431235
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 ANDA213248 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (46708-495-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • 30 TABLET, FILM COATED in 1 BOTTLE (46708-495-30)
  • 500 TABLET, FILM COATED in 1 BOTTLE (46708-495-71)
  • 90 TABLET, FILM COATED in 1 BOTTLE (46708-495-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (46708-495-91)
source: ndc

Packages (5)

Ingredients (1)

lurasidone hydrochloride (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a4f0715d-590f-4b13-bb72-19cdca95aa01", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["27f70e15-ee22-47ae-ba87-20e2b4a1a4d6"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (46708-495-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "46708-495-10", "marketing_start_date": "20230124"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (46708-495-30)", "package_ndc": "46708-495-30", "marketing_start_date": "20230124"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (46708-495-71)", "package_ndc": "46708-495-71", "marketing_start_date": "20230124"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (46708-495-90)", "package_ndc": "46708-495-90", "marketing_start_date": "20230124"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-495-91)", "package_ndc": "46708-495-91", "marketing_start_date": "20230124"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "46708-495_a4f0715d-590f-4b13-bb72-19cdca95aa01", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "46708-495", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA213248", "marketing_category": "ANDA", "marketing_start_date": "20230124", "listing_expiration_date": "20261231"}