Package 31722-004-90

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-004-90
Digits Only 3172200490
Product NDC 31722-004
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-004-90)

Marketing

Marketing Status
Marketed Since 2019-07-08
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1eee52e9-dda9-0d36-e063-6394a90a905b", "openfda": {"upc": ["0331722004305", "0331722002301", "0331722003308"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["0ee91447-2c23-4519-81cc-550b5416dd6b"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-004-01)  / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "31722-004-01", "marketing_start_date": "20190708"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-004-05)", "package_ndc": "31722-004-05", "marketing_start_date": "20190708"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-004-30)", "package_ndc": "31722-004-30", "marketing_start_date": "20190708"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-004-90)", "package_ndc": "31722-004-90", "marketing_start_date": "20190708"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "31722-004_1eee52e9-dda9-0d36-e063-6394a90a905b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "31722-004", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA212277", "marketing_category": "ANDA", "marketing_start_date": "20190708", "listing_expiration_date": "20261231"}