vilazodone hydrochloride

Generic: vilazodone hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vilazodone hydrochloride
Generic Name vilazodone hydrochloride
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

vilazodone hydrochloride 40 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-128
Product ID 82804-128_f68720fd-9122-4922-b472-733da8bd0a00
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208228
Listing Expiration 2026-12-31
Marketing Start 2023-10-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804128
Hyphenated Format 82804-128

Supplemental Identifiers

RxCUI
1086784
UPC
0382804128303
UNII
U8HTX2GK8J

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 ANDA208228 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (82804-128-30)
source: ndc

Packages (1)

82804-128-30 30 TABLET in 1 BOTTLE (82804-128-30)

Ingredients (1)

vilazodone hydrochloride (40 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": "f68720fd-9122-4922-b472-733da8bd0a00", "openfda": {"upc": ["0382804128303"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086784"], "spl_set_id": ["f68720fd-9122-4922-b472-733da8bd0a00"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-128-30)", "package_ndc": "82804-128-30", "marketing_start_date": "20240719"}], "brand_name": "vilazodone hydrochloride", "product_id": "82804-128_f68720fd-9122-4922-b472-733da8bd0a00", "dosage_form": "TABLET", "product_ndc": "82804-128", "generic_name": "vilazodone hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vilazodone hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208228", "marketing_category": "ANDA", "marketing_start_date": "20231026", "listing_expiration_date": "20261231"}