Package 68071-3886-3

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3886-3
Digits Only 6807138863
Product NDC 68071-3886
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3886-3)

Marketing

Marketing Status
Marketed Since 2025-08-19
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": "3cbe3e8f-3c54-cf73-e063-6294a90a4883", "openfda": {"upc": ["0368071388633"], "unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["3cbe3e18-9a7e-aaa3-e063-6394a90abf92"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3886-3)", "package_ndc": "68071-3886-3", "marketing_start_date": "20250819"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68071-3886_3cbe3e8f-3c54-cf73-e063-6294a90a4883", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-3886", "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": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}