Package 68071-5160-3

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-5160-3
Digits Only 6807151603
Product NDC 68071-5160
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-5160-3)

Marketing

Marketing Status
Marketed Since 2020-01-28
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": "1b56413d-bc89-9e3a-e063-6394a90afb19", "openfda": {"upc": ["0368071516036"], "unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["9d38eac0-9d64-1274-e053-2995a90a189a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-5160-3)", "package_ndc": "68071-5160-3", "marketing_start_date": "20200128"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68071-5160_1b56413d-bc89-9e3a-e063-6394a90afb19", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-5160", "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": "37.5 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}