venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: trigen laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler trigen laboratories, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 150 mg/1

Manufacturer
Trigen Laboratories, LLC

Identifiers & Regulatory

Product NDC 13811-714
Product ID 13811-714_55564637-0e7a-4684-be84-9d8c4cecacc3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA022104
Marketing Start 2010-04-29
Marketing End 2026-05-31

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 13811714
Hyphenated Format 13811-714

Supplemental Identifiers

RxCUI
808744 808748 808751 808753
UPC
0313811715309 0313811714302 0313811715903 0313811713305 0313811714906 0313811712902 0313811713909 0313811712308
UNII
7D7RX5A8MO

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

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-714-30)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-714-90)
source: ndc

Packages (2)

13811-714-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-714-30) 13811-714-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-714-90)

Ingredients (1)

venlafaxine hydrochloride (150 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": "55564637-0e7a-4684-be84-9d8c4cecacc3", "openfda": {"upc": ["0313811715309", "0313811714302", "0313811715903", "0313811713305", "0313811714906", "0313811712902", "0313811713909", "0313811712308"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["fdaed1c2-dd0a-4bf3-975a-86fe3e7f0c97"], "manufacturer_name": ["Trigen Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-714-30)", "package_ndc": "13811-714-30", "marketing_end_date": "20260531", "marketing_start_date": "20100429"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-714-90)", "package_ndc": "13811-714-90", "marketing_end_date": "20260531", "marketing_start_date": "20100429"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "13811-714_55564637-0e7a-4684-be84-9d8c4cecacc3", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "13811-714", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Trigen Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "NDA022104", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260531", "marketing_start_date": "20100429"}