Package 68071-3432-0

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 68071-3432-0
Digits Only 6807134320
Product NDC 68071-3432
Product ID 68071-3432_2d5887b5-8622-42a8-e063-6394a90a1b2e
Description

100 TABLET in 1 BOTTLE (68071-3432-0)

Marketing

Marketing Status
Marketed Since 2023-06-19
Brand venlafaxine
Generic venlafaxine
Sample Package No

Linked Drug Pages (1)

Venlafaxine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d5887b5-8622-42a8-e063-6394a90a1b2e", "openfda": {"upc": ["0368071343205"], "unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["fe7de51e-8a81-fe68-e053-6294a90a7339"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3432-0)", "package_ndc": "68071-3432-0", "marketing_start_date": "20230619"}], "brand_name": "Venlafaxine", "product_id": "68071-3432_2d5887b5-8622-42a8-e063-6394a90a1b2e", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-3432", "generic_name": "Venlafaxine", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}