vilazodone hydrochloride

Generic: vilazodone hydrochloride

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vilazodone hydrochloride
Generic Name vilazodone hydrochloride
Labeler northstar rx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

vilazodone hydrochloride 10 mg/1

Manufacturer
Northstar Rx LLC

Identifiers & Regulatory

Product NDC 72603-813
Product ID 72603-813_701c8b84-13ae-4adb-af7a-304bf1f21e3b
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 72603813
Hyphenated Format 72603-813

Supplemental Identifiers

RxCUI
1086772 1086778 1086784
UPC
0372603815016 0372603814019 0372603813012
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
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72603-813-01)
source: ndc

Packages (1)

Ingredients (1)

vilazodone hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "701c8b84-13ae-4adb-af7a-304bf1f21e3b", "openfda": {"upc": ["0372603815016", "0372603814019", "0372603813012"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["701c8b84-13ae-4adb-af7a-304bf1f21e3b"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72603-813-01)", "package_ndc": "72603-813-01", "marketing_start_date": "20250101"}], "brand_name": "vilazodone hydrochloride", "product_id": "72603-813_701c8b84-13ae-4adb-af7a-304bf1f21e3b", "dosage_form": "TABLET", "product_ndc": "72603-813", "generic_name": "vilazodone hydrochloride", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vilazodone hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208228", "marketing_category": "ANDA", "marketing_start_date": "20230707", "listing_expiration_date": "20261231"}