venlafaxine

Generic: venlafaxine

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 25 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-124
Product ID 82804-124_470ad045-6c82-4e44-8e88-0e2b01a41ff2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078932
Listing Expiration 2026-12-31
Marketing Start 2015-10-01

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 82804124
Hyphenated Format 82804-124

Supplemental Identifiers

RxCUI
313582
UPC
0382804124305
UNII
7D7RX5A8MO

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 ANDA078932 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (82804-124-30)
source: ndc

Packages (1)

82804-124-30 30 TABLET in 1 BOTTLE (82804-124-30)

Ingredients (1)

venlafaxine hydrochloride (25 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": "470ad045-6c82-4e44-8e88-0e2b01a41ff2", "openfda": {"upc": ["0382804124305"], "unii": ["7D7RX5A8MO"], "rxcui": ["313582"], "spl_set_id": ["470ad045-6c82-4e44-8e88-0e2b01a41ff2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-124-30)", "package_ndc": "82804-124-30", "marketing_start_date": "20240716"}], "brand_name": "venlafaxine", "product_id": "82804-124_470ad045-6c82-4e44-8e88-0e2b01a41ff2", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "82804-124", "generic_name": "venlafaxine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}