venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler coupler llc
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 150 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1656
Product ID 67046-1656_4a00703b-e5b8-ce3d-e063-6394a90a399e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217390
Listing Expiration 2027-12-31
Marketing Start 2026-02-04

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 670461656
Hyphenated Format 67046-1656

Supplemental Identifiers

RxCUI
313581
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 ANDA217390 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (67046-1656-3)
source: ndc

Packages (1)

67046-1656-3 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (67046-1656-3)

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": "4a00703b-e5b8-ce3d-e063-6394a90a399e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["4a007068-89d9-c296-e063-6394a90ad6d0"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (67046-1656-3)", "package_ndc": "67046-1656-3", "marketing_start_date": "20260204"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "67046-1656_4a00703b-e5b8-ce3d-e063-6394a90a399e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "67046-1656", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA217390", "marketing_category": "ANDA", "marketing_start_date": "20260204", "listing_expiration_date": "20271231"}