Package 50090-7324-0

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7324-0
Digits Only 5009073240
Product NDC 50090-7324
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7324-0)

Marketing

Marketing Status
Marketed Since 2024-10-15
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6187ee80-4138-4799-ae60-f0c6dfe7f2b3", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["0a1b6bcd-8d46-44ab-bc5d-65515601d2ff"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7324-0)", "package_ndc": "50090-7324-0", "marketing_start_date": "20241015"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "50090-7324_6187ee80-4138-4799-ae60-f0c6dfe7f2b3", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-7324", "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": "150 mg/1"}], "application_number": "ANDA214654", "marketing_category": "ANDA", "marketing_start_date": "20220907", "listing_expiration_date": "20261231"}