Package 68071-3653-9

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3653-9
Digits Only 6807136539
Product NDC 68071-3653
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3653-9)

Marketing

Marketing Status
Marketed Since 2024-07-24
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": "1e05152e-9c86-5068-e063-6294a90aa56e", "openfda": {"upc": ["0368071365399"], "unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["1e04fe02-88c9-dafd-e063-6294a90ac4c9"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3653-9)", "package_ndc": "68071-3653-9", "marketing_start_date": "20240724"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68071-3653_1e05152e-9c86-5068-e063-6294a90aa56e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-3653", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "labeler_name": "NuCare Pharmaceuticals, Inc.", "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"}