Package 50090-6599-0

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6599-0
Digits Only 5009065990
Product NDC 50090-6599
Product ID 50090-6599_59739442-2975-4203-997f-cf65cd63672b
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6599-0)

Marketing

Marketing Status
Marketed Since 2023-08-21
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "59739442-2975-4203-997f-cf65cd63672b", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["28c8f404-1dbd-4140-8959-32624d7c7724"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6599-0)", "package_ndc": "50090-6599-0", "marketing_start_date": "20230821"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "50090-6599_59739442-2975-4203-997f-cf65cd63672b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-6599", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}