Package 60760-728-60

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 60760-728-60
Digits Only 6076072860
Product NDC 60760-728
Product ID 60760-728_fab61465-dff5-0498-e053-6294a90a9aec
Description

60 TABLET in 1 BOTTLE, PLASTIC (60760-728-60)

Marketing

Marketing Status
Marketed Since 2023-04-21
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": "fab61465-dff5-0498-e053-6294a90a9aec", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313584"], "spl_set_id": ["fab65158-b2f7-1db7-e053-6294a90af231"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-728-60)", "package_ndc": "60760-728-60", "marketing_start_date": "20230421"}], "brand_name": "Venlafaxine", "product_id": "60760-728_fab61465-dff5-0498-e053-6294a90a9aec", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-728", "generic_name": "Venlafaxine", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "20230421", "listing_expiration_date": "20261231"}