vilazodone hydrochloride

Generic: vilazodone hydrochloride

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

Drug Facts

Product Profile

Brand Name vilazodone hydrochloride
Generic Name vilazodone hydrochloride
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

vilazodone hydrochloride 10 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-232
Product ID 62332-232_d97cafa3-ede7-49c6-bba1-6414e6968cb5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208202
Listing Expiration 2026-12-31
Marketing Start 2022-06-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332232
Hyphenated Format 62332-232

Supplemental Identifiers

RxCUI
1086772 1086778 1086784
UPC
0362332232307 0362332234301
UNII
U8HTX2GK8J

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 vilazodone hydrochloride (source: ndc)
Generic Name vilazodone hydrochloride (source: ndc)
Application Number ANDA208202 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (62332-232-30)
  • 500 TABLET, FILM COATED in 1 BOTTLE (62332-232-71)
  • 90 TABLET, FILM COATED in 1 BOTTLE (62332-232-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (62332-232-91)
source: ndc

Packages (4)

62332-232-30 30 TABLET, FILM COATED in 1 BOTTLE (62332-232-30) 62332-232-71 500 TABLET, FILM COATED in 1 BOTTLE (62332-232-71) 62332-232-90 90 TABLET, FILM COATED in 1 BOTTLE (62332-232-90) 62332-232-91 1000 TABLET, FILM COATED in 1 BOTTLE (62332-232-91)

Ingredients (1)

vilazodone hydrochloride (10 mg/1)

Linked Drug Pages (1)

VILAZODONE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d97cafa3-ede7-49c6-bba1-6414e6968cb5", "openfda": {"upc": ["0362332232307", "0362332234301"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["8b95b850-8bdf-4255-a691-783d1a94bd07"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-232-30)", "package_ndc": "62332-232-30", "marketing_start_date": "20220604"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62332-232-71)", "package_ndc": "62332-232-71", "marketing_start_date": "20220604"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62332-232-90)", "package_ndc": "62332-232-90", "marketing_start_date": "20220604"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-232-91)", "package_ndc": "62332-232-91", "marketing_start_date": "20220604"}], "brand_name": "VILAZODONE HYDROCHLORIDE", "product_id": "62332-232_d97cafa3-ede7-49c6-bba1-6414e6968cb5", "dosage_form": "TABLET, FILM COATED", "product_ndc": "62332-232", "generic_name": "VILAZODONE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VILAZODONE HYDROCHLORIDE", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208202", "marketing_category": "ANDA", "marketing_start_date": "20220604", "listing_expiration_date": "20261231"}