venlafaxine

Generic: venlafaxine

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-249
Product ID 23155-249_a94fad9c-da90-46ad-8644-f956976a6556
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078554
Listing Expiration 2026-12-31
Marketing Start 2021-07-19

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 23155249
Hyphenated Format 23155-249

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 (source: ndc)
Application Number ANDA078554 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-249-01)
  • 90 TABLET in 1 BOTTLE (23155-249-09)
source: ndc

Packages (2)

23155-249-01 100 TABLET in 1 BOTTLE (23155-249-01) 23155-249-09 90 TABLET in 1 BOTTLE (23155-249-09)

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": "a94fad9c-da90-46ad-8644-f956976a6556", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["80ac757d-c629-4579-8afd-cae0ee9cd614"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-249-01)", "package_ndc": "23155-249-01", "marketing_start_date": "20210719"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (23155-249-09)", "package_ndc": "23155-249-09", "marketing_start_date": "20210719"}], "brand_name": "VENLAFAXINE", "product_id": "23155-249_a94fad9c-da90-46ad-8644-f956976a6556", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "23155-249", "generic_name": "VENLAFAXINE", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA078554", "marketing_category": "ANDA", "marketing_start_date": "20210719", "listing_expiration_date": "20261231"}