Package 76420-630-30
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
76420-630-30
Digits Only
7642063030
Product NDC
76420-630
Description
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-630-30)
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": "2ef15b5a-edd3-27a8-e063-6394a90a2aa3", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["c69d16fd-b82d-4708-aece-ab4f60b29cc6"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-630-01)", "package_ndc": "76420-630-01", "marketing_start_date": "20231018"}, {"sample": false, "description": "15 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-630-15)", "package_ndc": "76420-630-15", "marketing_start_date": "20231018"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-630-30)", "package_ndc": "76420-630-30", "marketing_start_date": "20231018"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-630-60)", "package_ndc": "76420-630-60", "marketing_start_date": "20231018"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (76420-630-90)", "package_ndc": "76420-630-90", "marketing_start_date": "20231018"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "76420-630_2ef15b5a-edd3-27a8-e063-6394a90a2aa3", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "76420-630", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "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"}