venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: advanced rx of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler advanced rx of tennessee, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Advanced Rx of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0477
Product ID 80425-0477_2d034ebe-1e07-6fe0-e063-6394a90a368b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA022104
Listing Expiration 2026-12-31
Marketing Start 2025-01-30

Pharmacologic Class

Classes
norepinephrine uptake inhibitors [moa] serotonin uptake inhibitors [moa] serotonin and norepinephrine reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250477
Hyphenated Format 80425-0477

Supplemental Identifiers

RxCUI
808751
UNII
7D7RX5A8MO

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 venlafaxine hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number NDA022104 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-1)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-2)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-3)
source: ndc

Packages (3)

80425-0477-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-1) 80425-0477-2 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-2) 80425-0477-3 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-3)

Ingredients (1)

venlafaxine hydrochloride (37.5 mg/1)

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d034ebe-1e07-6fe0-e063-6394a90a368b", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808751"], "spl_set_id": ["2cf6e6ad-7d00-0db1-e063-6394a90ab1ec"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-1)", "package_ndc": "80425-0477-1", "marketing_start_date": "20250130"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-2)", "package_ndc": "80425-0477-2", "marketing_start_date": "20250130"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-3)", "package_ndc": "80425-0477-3", "marketing_start_date": "20250130"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "80425-0477_2d034ebe-1e07-6fe0-e063-6394a90a368b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "80425-0477", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "NDA022104", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20250130", "listing_expiration_date": "20261231"}