Package 72162-1089-3

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1089-3
Digits Only 7216210893
Product NDC 72162-1089
Product ID 72162-1089_e2c3a496-9960-4eec-896f-eb7bf41ba23e
Description

30 TABLET in 1 BOTTLE (72162-1089-3)

Marketing

Marketing Status
Marketed Since 2023-10-09
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": "e2c3a496-9960-4eec-896f-eb7bf41ba23e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744"], "spl_set_id": ["700d2c21-b5be-4d24-98a5-dc456ef42857"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1089-3)", "package_ndc": "72162-1089-3", "marketing_start_date": "20231009"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "72162-1089_e2c3a496-9960-4eec-896f-eb7bf41ba23e", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72162-1089", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA209193", "marketing_category": "ANDA", "marketing_start_date": "20191226", "listing_expiration_date": "20261231"}