vilazodone hydrochloride

Generic: vilazodone hydrochloride

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vilazodone hydrochloride
Generic Name vilazodone hydrochloride
Labeler novadoz pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

vilazodone hydrochloride 20 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-261
Product ID 72205-261_c3e167cd-7f56-45eb-80df-a60fa1392e57
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208228
Listing Expiration 2026-12-31
Marketing Start 2023-07-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205261
Hyphenated Format 72205-261

Supplemental Identifiers

RxCUI
1086772 1086778 1086784
UPC
0372205262300 0372205261303 0372205260306
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 ANDA208228 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72205-261-30)
source: ndc

Packages (1)

Ingredients (1)

vilazodone hydrochloride (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c3e167cd-7f56-45eb-80df-a60fa1392e57", "openfda": {"upc": ["0372205262300", "0372205261303", "0372205260306"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["c3e167cd-7f56-45eb-80df-a60fa1392e57"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72205-261-30)", "package_ndc": "72205-261-30", "marketing_start_date": "20230714"}], "brand_name": "vilazodone hydrochloride", "product_id": "72205-261_c3e167cd-7f56-45eb-80df-a60fa1392e57", "dosage_form": "TABLET", "product_ndc": "72205-261", "generic_name": "vilazodone hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vilazodone hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208228", "marketing_category": "ANDA", "marketing_start_date": "20230707", "listing_expiration_date": "20261231"}