vilazodone hydrochloride
Generic: vilazodone hydrochloride
Labeler: novadoz pharmaceuticals llcDrug Facts
Product Profile
Brand Name
vilazodone hydrochloride
Generic Name
vilazodone hydrochloride
Labeler
novadoz pharmaceuticals llc
Dosage Form
TABLET
Routes
Active Ingredients
vilazodone hydrochloride 20 mg/1
Manufacturer
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
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (72205-261-30)
Packages (1)
Ingredients (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"}