Package 70771-1838-4
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
70771-1838-4
Digits Only
7077118384
Product NDC
70771-1838
Description
10 BLISTER PACK in 1 CARTON (70771-1838-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70771-1838-2)
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": "665f7293-1792-4b57-b8af-3e1fc33e8200", "openfda": {"upc": ["0370771183890"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["1349bace-d2cb-4c8f-8cbd-c09e67a2ca1b"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1838-0)", "package_ndc": "70771-1838-0", "marketing_start_date": "20230518"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1838-3)", "package_ndc": "70771-1838-3", "marketing_start_date": "20230518"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1838-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70771-1838-2)", "package_ndc": "70771-1838-4", "marketing_start_date": "20230518"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1838-5)", "package_ndc": "70771-1838-5", "marketing_start_date": "20230518"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1838-9)", "package_ndc": "70771-1838-9", "marketing_start_date": "20230518"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "70771-1838_665f7293-1792-4b57-b8af-3e1fc33e8200", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70771-1838", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA090174", "marketing_category": "ANDA", "marketing_start_date": "20230518", "listing_expiration_date": "20261231"}