venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: vertical pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler vertical pharmaceuticals, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Vertical Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 68025-079
Product ID 68025-079_499e9472-5d08-4d56-8dbc-f1a4b632631e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA022104
Marketing Start 2010-04-29
Marketing End 2026-03-31

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 68025079
Hyphenated Format 68025-079

Supplemental Identifiers

RxCUI
808744 808748 808751 808753
UPC
0368025082303 0368025080309 0368025079303 0368025081306
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 hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number NDA022104 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-079-30)
source: ndc

Packages (1)

68025-079-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-079-30)

Ingredients (1)

venlafaxine hydrochloride (37.5 mg/1)

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "499e9472-5d08-4d56-8dbc-f1a4b632631e", "openfda": {"upc": ["0368025082303", "0368025080309", "0368025079303", "0368025081306"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["82872e90-4f86-49f7-9f38-39c0f75e4467"], "manufacturer_name": ["Vertical Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-079-30)", "package_ndc": "68025-079-30", "marketing_end_date": "20260331", "marketing_start_date": "20100429"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68025-079_499e9472-5d08-4d56-8dbc-f1a4b632631e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68025-079", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Vertical Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "NDA022104", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260331", "marketing_start_date": "20100429"}