venlafaxine

Generic: venlafaxine

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler zydus pharmaceuticals usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 68382-021
Product ID 68382-021_ea404f6c-7e07-4779-a52c-8cffb92718ef
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 68382021
Hyphenated Format 68382-021

Supplemental Identifiers

RxCUI
313580 313582 313584 313586 314277
UPC
0368382019011 0368382018014 0368382021014 0368382101013
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 ANDA077653 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68382-021-01)
  • 500 TABLET in 1 BOTTLE (68382-021-05)
  • 30 TABLET in 1 BOTTLE (68382-021-06)
  • 1000 TABLET in 1 BOTTLE (68382-021-10)
  • 60 TABLET in 1 BOTTLE (68382-021-14)
  • 90 TABLET in 1 BOTTLE (68382-021-16)
source: ndc

Packages (6)

68382-021-01 100 TABLET in 1 BOTTLE (68382-021-01) 68382-021-05 500 TABLET in 1 BOTTLE (68382-021-05) 68382-021-06 30 TABLET in 1 BOTTLE (68382-021-06) 68382-021-10 1000 TABLET in 1 BOTTLE (68382-021-10) 68382-021-14 60 TABLET in 1 BOTTLE (68382-021-14) 68382-021-16 90 TABLET in 1 BOTTLE (68382-021-16)

Ingredients (1)

venlafaxine hydrochloride (75 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": "ea404f6c-7e07-4779-a52c-8cffb92718ef", "openfda": {"upc": ["0368382019011", "0368382018014", "0368382021014", "0368382101013"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["72efad5f-0909-46a5-aa13-ac24fe015fe6"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-021-01)", "package_ndc": "68382-021-01", "marketing_start_date": "20080613"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68382-021-05)", "package_ndc": "68382-021-05", "marketing_start_date": "20080613"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68382-021-06)", "package_ndc": "68382-021-06", "marketing_start_date": "20080613"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68382-021-10)", "package_ndc": "68382-021-10", "marketing_start_date": "20080613"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68382-021-14)", "package_ndc": "68382-021-14", "marketing_start_date": "20080613"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68382-021-16)", "package_ndc": "68382-021-16", "marketing_start_date": "20080613"}], "brand_name": "Venlafaxine", "product_id": "68382-021_ea404f6c-7e07-4779-a52c-8cffb92718ef", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68382-021", "generic_name": "Venlafaxine", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}