vilazodone hydrochloride

Generic: vilazodone hydrochloride

Labeler: cipla usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

vilazodone hydrochloride 20 mg/1

Manufacturer
Cipla USA Inc.

Identifiers & Regulatory

Product NDC 69097-981
Product ID 69097-981_e16f2d8b-a5ec-498f-97c4-d1c9d897140f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208200
Listing Expiration 2026-12-31
Marketing Start 2023-01-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69097981
Hyphenated Format 69097-981

Supplemental Identifiers

RxCUI
1086772 1086778 1086784
UPC
0369097981020 0369097979027 0369097982027
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 ANDA208200 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (69097-981-02)
source: ndc

Packages (1)

69097-981-02 30 TABLET, FILM COATED in 1 BOTTLE (69097-981-02)

Ingredients (1)

vilazodone hydrochloride (20 mg/1)

Linked Drug Pages (1)

Vilazodone Hydrochloride, Vilazodone hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e16f2d8b-a5ec-498f-97c4-d1c9d897140f", "openfda": {"upc": ["0369097981020", "0369097979027", "0369097982027"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["658c4bc1-4128-4e0e-8852-b5f68880e8d7"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69097-981-02)", "package_ndc": "69097-981-02", "marketing_start_date": "20230123"}], "brand_name": "Vilazodone hydrochloride", "product_id": "69097-981_e16f2d8b-a5ec-498f-97c4-d1c9d897140f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "69097-981", "generic_name": "Vilazodone hydrochloride", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vilazodone hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208200", "marketing_category": "ANDA", "marketing_start_date": "20230123", "listing_expiration_date": "20261231"}