Package 43598-001-90
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
43598-001-90
Digits Only
4359800190
Product NDC
43598-001
Description
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-90)
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": "646ca48a-403a-0ef0-0fc2-a5569c5b70fd", "openfda": {"upc": ["0343598001302", "0343598999302"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["f5c21429-d5d0-9f93-a465-6e5e0e19ebdd"], "manufacturer_name": ["Dr.Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-10)", "package_ndc": "43598-001-10", "marketing_start_date": "20240909"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-30)", "package_ndc": "43598-001-30", "marketing_start_date": "20240909"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-001-90)", "package_ndc": "43598-001-90", "marketing_start_date": "20240909"}], "brand_name": "venlafaxine hydrochloride", "product_id": "43598-001_646ca48a-403a-0ef0-0fc2-a5569c5b70fd", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "43598-001", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Dr.Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA078421", "marketing_category": "ANDA", "marketing_start_date": "20240909", "listing_expiration_date": "20261231"}