Package 65862-527-90
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
65862-527-90
Digits Only
6586252790
Product NDC
65862-527
Description
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-90)
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 (65862-527-01)", "package_ndc": "65862-527-01", "marketing_start_date": "20110601"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-527-10) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "65862-527-10", "marketing_start_date": "20110601"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-30)", "package_ndc": "65862-527-30", "marketing_start_date": "20110601"}, {"sample": false, "description": "15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-47)", "package_ndc": "65862-527-47", "marketing_start_date": "20110601"}, {"sample": false, "description": "5000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-59)", "package_ndc": "65862-527-59", "marketing_start_date": "20110601"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-90)", "package_ndc": "65862-527-90", "marketing_start_date": "20110601"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65862-527-99)", "package_ndc": "65862-527-99", "marketing_start_date": "20110601"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "65862-527_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": "65862-527", "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": "37.5 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}