venlafaxine

Generic: venlafaxine

Labeler: dr. reddy's laboratories inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler dr. reddy's laboratories inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 225 mg/1

Manufacturer
Dr. Reddy's Laboratories Inc.

Identifiers & Regulatory

Product NDC 43598-944
Product ID 43598-944_79d34297-6604-4031-a89a-8ec557d078d1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214609
Listing Expiration 2026-12-31
Marketing Start 2021-09-20

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 43598944
Hyphenated Format 43598-944

Supplemental Identifiers

RxCUI
808744 808748
UPC
0343598943909 0343598944906 0343598944302 0343598943305
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 (source: ndc)
Generic Name venlafaxine (source: ndc)
Application Number ANDA214609 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 225 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-30)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-90)
source: ndc

Packages (2)

43598-944-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-30) 43598-944-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-90)

Ingredients (1)

venlafaxine hydrochloride (225 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": "79d34297-6604-4031-a89a-8ec557d078d1", "openfda": {"upc": ["0343598943909", "0343598944906", "0343598944302", "0343598943305"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748"], "spl_set_id": ["9312f4df-63d9-4167-880f-36a816870442"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-30)", "package_ndc": "43598-944-30", "marketing_start_date": "20210920"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-90)", "package_ndc": "43598-944-90", "marketing_start_date": "20210920"}], "brand_name": "Venlafaxine", "product_id": "43598-944_79d34297-6604-4031-a89a-8ec557d078d1", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "43598-944", "generic_name": "Venlafaxine", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA214609", "marketing_category": "ANDA", "marketing_start_date": "20210920", "listing_expiration_date": "20261231"}