Package 70518-2659-0

Brand: venlafaxine

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2659-0
Digits Only 7051826590
Product NDC 70518-2659
Product ID 70518-2659_4a7cd961-c6d4-a553-e063-6394a90af209
Description

30 TABLET in 1 BLISTER PACK (70518-2659-0)

Marketing

Marketing Status
Marketed Since 2020-03-27
Brand venlafaxine
Generic venlafaxine hydrochloride
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": "4a7cd961-c6d4-a553-e063-6394a90af209", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313582"], "spl_set_id": ["ddb51556-0292-4aa9-b781-a402c912591f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2659-0)", "package_ndc": "70518-2659-0", "marketing_start_date": "20200327"}], "brand_name": "venlafaxine", "product_id": "70518-2659_4a7cd961-c6d4-a553-e063-6394a90af209", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2659", "generic_name": "venlafaxine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20200327", "listing_expiration_date": "20271231"}