venlafaxine

Generic: venlafaxine

Labeler: modavar pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler modavar pharmaceuticals llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
Modavar Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72241-075
Product ID 72241-075_14b38374-7287-47dd-8ef9-e88bd5b23a26
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211323
Listing Expiration 2026-12-31
Marketing Start 2018-01-05

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 72241075
Hyphenated Format 72241-075

Supplemental Identifiers

RxCUI
808744 808748 808753
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 ANDA211323 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 90 TABLET, COATED in 1 BOTTLE (72241-075-04)
  • 1000 TABLET, COATED in 1 BOTTLE (72241-075-11)
  • 30 TABLET, COATED in 1 BOTTLE (72241-075-22)
source: ndc

Packages (3)

72241-075-04 90 TABLET, COATED in 1 BOTTLE (72241-075-04) 72241-075-11 1000 TABLET, COATED in 1 BOTTLE (72241-075-11) 72241-075-22 30 TABLET, COATED in 1 BOTTLE (72241-075-22)

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": "14b38374-7287-47dd-8ef9-e88bd5b23a26", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808753"], "spl_set_id": ["14b38374-7287-47dd-8ef9-e88bd5b23a26"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (72241-075-04)", "package_ndc": "72241-075-04", "marketing_start_date": "20180816"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (72241-075-11)", "package_ndc": "72241-075-11", "marketing_start_date": "20180816"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72241-075-22)", "package_ndc": "72241-075-22", "marketing_start_date": "20180816"}], "brand_name": "Venlafaxine", "product_id": "72241-075_14b38374-7287-47dd-8ef9-e88bd5b23a26", "dosage_form": "TABLET, COATED", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72241-075", "generic_name": "Venlafaxine", "labeler_name": "Modavar Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA211323", "marketing_category": "ANDA", "marketing_start_date": "20180105", "listing_expiration_date": "20261231"}