Package 50090-7319-0
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
50090-7319-0
Digits Only
5009073190
Product NDC
50090-7319
Description
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7319-0)
Marketing
Marketing Status
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": "d4f02f0c-6337-4eff-906d-1f4aa482a600", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["d94e5404-f728-4e4b-af99-8a8e4dfae227"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7319-0)", "package_ndc": "50090-7319-0", "marketing_start_date": "20241014"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "50090-7319_d4f02f0c-6337-4eff-906d-1f4aa482a600", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-7319", "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": "ANDA214654", "marketing_category": "ANDA", "marketing_start_date": "20220907", "listing_expiration_date": "20261231"}