effexor xr

Generic: venlafaxine hydrochloride

Labeler: viatris specialty llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name effexor xr
Generic Name venlafaxine hydrochloride
Labeler viatris specialty llc
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 150 mg/1

Manufacturer
Viatris Specialty LLC

Identifiers & Regulatory

Product NDC 58151-127
Product ID 58151-127_2319042f-5d24-42d3-9b0a-8893bed66813
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020699
Listing Expiration 2026-12-31
Marketing Start 2024-08-01

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 58151127
Hyphenated Format 58151-127

Supplemental Identifiers

RxCUI
313581 313583 313585 729929 729931 729932
UPC
0358151126934 0358151125937 0358151127931
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 effexor xr (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number NDA020699 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-77)
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-93)
source: ndc

Packages (2)

58151-127-77 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-77) 58151-127-93 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-93)

Ingredients (1)

venlafaxine hydrochloride (150 mg/1)

Linked Drug Pages (1)

Effexor XR ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2319042f-5d24-42d3-9b0a-8893bed66813", "openfda": {"upc": ["0358151126934", "0358151125937", "0358151127931"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585", "729929", "729931", "729932"], "spl_set_id": ["c848a5d8-ba94-4c84-80e3-0bf35fb8e32e"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-77)", "package_ndc": "58151-127-77", "marketing_start_date": "20240801"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-93)", "package_ndc": "58151-127-93", "marketing_start_date": "20250701"}], "brand_name": "Effexor XR", "product_id": "58151-127_2319042f-5d24-42d3-9b0a-8893bed66813", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "58151-127", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Effexor", "brand_name_suffix": "XR", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "NDA020699", "marketing_category": "NDA", "marketing_start_date": "20240801", "listing_expiration_date": "20261231"}