Package 71610-606-17

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 71610-606-17
Digits Only 7161060617
Product NDC 71610-606
Product ID 71610-606_530e3bfa-2893-4f97-815c-b943e8d2415d
Description

6030 TABLET in 1 BOTTLE (71610-606-17)

Marketing

Marketing Status
Marketed Since 2021-10-25
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": "530e3bfa-2893-4f97-815c-b943e8d2415d", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["2887a463-2da1-4f8d-afef-f4c88d31e04d"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "6030 TABLET in 1 BOTTLE (71610-606-17)", "package_ndc": "71610-606-17", "marketing_start_date": "20211025"}], "brand_name": "Venlafaxine", "product_id": "71610-606_530e3bfa-2893-4f97-815c-b943e8d2415d", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71610-606", "generic_name": "Venlafaxine", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA078627", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}