Package 68071-3431-0

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 68071-3431-0
Digits Only 6807134310
Product NDC 68071-3431
Product ID 68071-3431_2d58848f-040e-c4bd-e063-6294a90a33e4
Description

100 TABLET in 1 BOTTLE (68071-3431-0)

Marketing

Marketing Status
Marketed Since 2023-07-27
Brand venlafaxine
Generic venlafaxine
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d58848f-040e-c4bd-e063-6294a90a33e4", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313584"], "spl_set_id": ["017a84aa-0e1f-f560-e063-6294a90a9069"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3431-0)", "package_ndc": "68071-3431-0", "marketing_start_date": "20230727"}], "brand_name": "Venlafaxine", "product_id": "68071-3431_2d58848f-040e-c4bd-e063-6294a90a33e4", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-3431", "generic_name": "Venlafaxine", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}