Package 65862-697-05
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
65862-697-05
Digits Only
6586269705
Product NDC
65862-697
Description
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-05)
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": "d3f9b554-05be-484f-b9e7-5c8e6b2de9c9", "openfda": {"upc": ["0365862528476", "0365862527479"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["85d3ce8b-8966-45d9-bdaf-f6f0475096e1"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-01)", "package_ndc": "65862-697-01", "marketing_start_date": "20111123"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-05)", "package_ndc": "65862-697-05", "marketing_start_date": "20111123"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-697-10) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "65862-697-10", "marketing_start_date": "20111123"}, {"sample": false, "description": "2500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-26)", "package_ndc": "65862-697-26", "marketing_start_date": "20111123"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-30)", "package_ndc": "65862-697-30", "marketing_start_date": "20111123"}, {"sample": false, "description": "15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-47)", "package_ndc": "65862-697-47", "marketing_start_date": "20111123"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-697-90)", "package_ndc": "65862-697-90", "marketing_start_date": "20111123"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "65862-697_d3f9b554-05be-484f-b9e7-5c8e6b2de9c9", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "65862-697", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20111123", "listing_expiration_date": "20261231"}