venlafaxine

Generic: venlafaxine

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

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler remedyrepack inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 150 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4500
Product ID 70518-4500_4109ea54-b204-364e-e063-6394a90a0b9a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214127
Listing Expiration 2026-12-31
Marketing Start 2025-10-12

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 705184500
Hyphenated Format 70518-4500

Supplemental Identifiers

RxCUI
808744
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 (source: ndc)
Generic Name venlafaxine (source: ndc)
Application Number ANDA214127 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4500-0)
source: ndc

Packages (1)

70518-4500-0 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4500-0)

Ingredients (1)

venlafaxine hydrochloride (150 mg/1)

Linked Drug Pages (1)

Venlafaxine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4109ea54-b204-364e-e063-6394a90a0b9a", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744"], "spl_set_id": ["4b23e4bd-b6ab-42f2-b389-0be0b7e11b92"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4500-0)", "package_ndc": "70518-4500-0", "marketing_start_date": "20251012"}], "brand_name": "Venlafaxine", "product_id": "70518-4500_4109ea54-b204-364e-e063-6394a90a0b9a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-4500", "generic_name": "Venlafaxine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA214127", "marketing_category": "ANDA", "marketing_start_date": "20251012", "listing_expiration_date": "20261231"}