Package 71785-1006-3

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71785-1006-3
Digits Only 7178510063
Product NDC 71785-1006
Description

10 BLISTER PACK in 1 CARTON (71785-1006-3) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-07-08
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": "b45cbdea-d1be-c16d-e053-2a95a90a821e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["e901e476-58bd-4204-baaa-a4634ae65ab3"], "manufacturer_name": ["Annora Pharma Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71785-1006-0)", "package_ndc": "71785-1006-0", "marketing_start_date": "20190708"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71785-1006-1)", "package_ndc": "71785-1006-1", "marketing_start_date": "20190708"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71785-1006-2)", "package_ndc": "71785-1006-2", "marketing_start_date": "20190708"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (71785-1006-3)  / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "71785-1006-3", "marketing_start_date": "20190708"}], "brand_name": "VENLAFAXINE HYDROCHLORIDE", "product_id": "71785-1006_b45cbdea-d1be-c16d-e053-2a95a90a821e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71785-1006", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "labeler_name": "Annora Pharma Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE HYDROCHLORIDE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA212277", "marketing_category": "ANDA", "marketing_start_date": "20190708", "listing_expiration_date": "20261231"}