Package 50090-4865-0

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 50090-4865-0
Digits Only 5009048650
Product NDC 50090-4865
Description

30 TABLET in 1 BOTTLE (50090-4865-0)

Marketing

Marketing Status
Marketed Since 2020-01-23
Brand venlafaxine
Generic venlafaxine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47cfd5a6-1c1a-4e5f-97f5-9ab1c7b218a4", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313584"], "spl_set_id": ["7bbdc9c5-a4b9-44d4-babc-46bd8c2e084a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-4865-0)", "package_ndc": "50090-4865-0", "marketing_start_date": "20200123"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4865-1)", "package_ndc": "50090-4865-1", "marketing_start_date": "20200123"}], "brand_name": "Venlafaxine", "product_id": "50090-4865_47cfd5a6-1c1a-4e5f-97f5-9ab1c7b218a4", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-4865", "generic_name": "Venlafaxine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}