venlafaxine

Generic: venlafaxine

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler bluepoint laboratories
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 50 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-159
Product ID 68001-159_04c5d11d-d249-eb93-e063-6294a90a1b46
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077653
Listing Expiration 2026-12-31
Marketing Start 2013-11-25

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 68001159
Hyphenated Format 68001-159

Supplemental Identifiers

RxCUI
313580 313582 313584 313586 314277
UPC
0368001156004 0368001157001 0368001160001 0368001158008 0368001159005
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
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68001-159-00)
source: ndc

Packages (1)

68001-159-00 100 TABLET in 1 BOTTLE (68001-159-00)

Ingredients (1)

venlafaxine hydrochloride (50 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": "04c5d11d-d249-eb93-e063-6294a90a1b46", "openfda": {"upc": ["0368001156004", "0368001157001", "0368001160001", "0368001158008", "0368001159005"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["172b3d3d-bdae-47bf-8fba-edd6da1a8649"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-159-00)", "package_ndc": "68001-159-00", "marketing_start_date": "20131125"}], "brand_name": "Venlafaxine", "product_id": "68001-159_04c5d11d-d249-eb93-e063-6294a90a1b46", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68001-159", "generic_name": "Venlafaxine", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20131125", "listing_expiration_date": "20261231"}