Package 65841-751-10
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
65841-751-10
Digits Only
6584175110
Product NDC
65841-751
Description
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-10)
Marketing
Marketing Status
Brand
venlafaxine hydrochloride
Generic
venlafaxine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f20749dc-d1f6-4860-b583-82b82d3a2242", "openfda": {"upc": ["0365841752106", "0365841753103"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["1be1be3a-304b-4e31-8732-335247029191"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-06)", "package_ndc": "65841-751-06", "marketing_start_date": "20110601"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-10)", "package_ndc": "65841-751-10", "marketing_start_date": "20110601"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-16)", "package_ndc": "65841-751-16", "marketing_start_date": "20110601"}], "brand_name": "venlafaxine hydrochloride", "product_id": "65841-751_f20749dc-d1f6-4860-b583-82b82d3a2242", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "65841-751", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA090174", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}