Package 68025-079-30

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68025-079-30
Digits Only 6802507930
Product NDC 68025-079
Product ID 68025-079_499e9472-5d08-4d56-8dbc-f1a4b632631e
Description

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

Marketing

Marketing Status
Discontinued 2026-03-31
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.95)

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"}