venlafaxine

Generic: venlafaxine hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine hydrochloride
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-405
Product ID 65862-405_426d12db-50e2-4915-999f-84645fb387d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090555
Listing Expiration 2026-12-31
Marketing Start 2010-04-07

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 65862405
Hyphenated Format 65862-405

Supplemental Identifiers

RxCUI
313580 313582 313584 313586 314277
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 hydrochloride (source: ndc)
Application Number ANDA090555 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (65862-405-01)
  • 10 BLISTER PACK in 1 CARTON (65862-405-10) / 10 TABLET in 1 BLISTER PACK
  • 30 TABLET in 1 BOTTLE (65862-405-30)
  • 60 TABLET in 1 BOTTLE (65862-405-60)
  • 6000 TABLET in 1 BOTTLE (65862-405-66)
  • 90 TABLET in 1 BOTTLE (65862-405-90)
  • 1000 TABLET in 1 BOTTLE (65862-405-99)
source: ndc

Packages (7)

65862-405-01 100 TABLET in 1 BOTTLE (65862-405-01) 65862-405-10 10 BLISTER PACK in 1 CARTON (65862-405-10) / 10 TABLET in 1 BLISTER PACK 65862-405-30 30 TABLET in 1 BOTTLE (65862-405-30) 65862-405-60 60 TABLET in 1 BOTTLE (65862-405-60) 65862-405-66 6000 TABLET in 1 BOTTLE (65862-405-66) 65862-405-90 90 TABLET in 1 BOTTLE (65862-405-90) 65862-405-99 1000 TABLET in 1 BOTTLE (65862-405-99)

Ingredients (1)

venlafaxine hydrochloride (37.5 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": "426d12db-50e2-4915-999f-84645fb387d9", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["b23637e5-d37f-41b5-ba76-fc053e903bc2"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-405-01)", "package_ndc": "65862-405-01", "marketing_start_date": "20100407"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-405-10)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "65862-405-10", "marketing_start_date": "20100407"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65862-405-30)", "package_ndc": "65862-405-30", "marketing_start_date": "20100407"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (65862-405-60)", "package_ndc": "65862-405-60", "marketing_start_date": "20100407"}, {"sample": false, "description": "6000 TABLET in 1 BOTTLE (65862-405-66)", "package_ndc": "65862-405-66", "marketing_start_date": "20100407"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65862-405-90)", "package_ndc": "65862-405-90", "marketing_start_date": "20100407"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-405-99)", "package_ndc": "65862-405-99", "marketing_start_date": "20100407"}], "brand_name": "Venlafaxine", "product_id": "65862-405_426d12db-50e2-4915-999f-84645fb387d9", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "65862-405", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20100407", "listing_expiration_date": "20261231"}