Package 68071-2990-9

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 68071-2990-9
Digits Only 6807129909
Product NDC 68071-2990
Product ID 68071-2990_37268d22-d0e6-36a5-e063-6294a90a46c2
Description

90 TABLET in 1 BOTTLE (68071-2990-9)

Marketing

Marketing Status
Marketed Since 2023-04-24
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": "37268d22-d0e6-36a5-e063-6294a90a46c2", "openfda": {"upc": ["0368071299090"], "unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["fa1db21b-98b8-3bde-e053-6394a90aa638"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-2990-9)", "package_ndc": "68071-2990-9", "marketing_start_date": "20230424"}], "brand_name": "Venlafaxine", "product_id": "68071-2990_37268d22-d0e6-36a5-e063-6294a90a46c2", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-2990", "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"}