venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler zydus lifesciences limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 65841-672
Product ID 65841-672_d4325db5-166d-4719-bdbd-a89ef8c96833
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077653
Listing Expiration 2026-12-31
Marketing Start 2008-06-13

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 65841672
Hyphenated Format 65841-672

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 hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number ANDA077653 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (65841-672-01)
  • 500 TABLET in 1 BOTTLE (65841-672-05)
  • 30 TABLET in 1 BOTTLE (65841-672-06)
  • 1000 TABLET in 1 BOTTLE (65841-672-10)
  • 60 TABLET in 1 BOTTLE (65841-672-14)
  • 90 TABLET in 1 BOTTLE (65841-672-16)
source: ndc

Packages (6)

65841-672-01 100 TABLET in 1 BOTTLE (65841-672-01) 65841-672-05 500 TABLET in 1 BOTTLE (65841-672-05) 65841-672-06 30 TABLET in 1 BOTTLE (65841-672-06) 65841-672-10 1000 TABLET in 1 BOTTLE (65841-672-10) 65841-672-14 60 TABLET in 1 BOTTLE (65841-672-14) 65841-672-16 90 TABLET in 1 BOTTLE (65841-672-16)

Ingredients (1)

venlafaxine hydrochloride (37.5 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": "d4325db5-166d-4719-bdbd-a89ef8c96833", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["51334651-7a7f-4653-bf9d-d5be04fd902d"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65841-672-01)", "package_ndc": "65841-672-01", "marketing_start_date": "20080613"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65841-672-05)", "package_ndc": "65841-672-05", "marketing_start_date": "20080613"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65841-672-06)", "package_ndc": "65841-672-06", "marketing_start_date": "20080613"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65841-672-10)", "package_ndc": "65841-672-10", "marketing_start_date": "20080613"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (65841-672-14)", "package_ndc": "65841-672-14", "marketing_start_date": "20080613"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65841-672-16)", "package_ndc": "65841-672-16", "marketing_start_date": "20080613"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "65841-672_d4325db5-166d-4719-bdbd-a89ef8c96833", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "65841-672", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}