Package 60760-713-30

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 60760-713-30
Digits Only 6076071330
Product NDC 60760-713
Product ID 60760-713_d27f6885-dc43-90c1-e053-2995a90a6526
Description

30 TABLET in 1 BOTTLE, PLASTIC (60760-713-30)

Marketing

Marketing Status
Marketed Since 2018-09-27
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": "d27f6885-dc43-90c1-e053-2995a90a6526", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["70d47b50-5722-3868-e053-2991aa0af85e"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-713-30)", "package_ndc": "60760-713-30", "marketing_start_date": "20180927"}], "brand_name": "venlafaxine", "product_id": "60760-713_d27f6885-dc43-90c1-e053-2995a90a6526", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-713", "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": "75 mg/1"}], "application_number": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20180712", "listing_expiration_date": "20261231"}