Package 62332-794-31

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62332-794-31
Digits Only 6233279431
Product NDC 62332-794
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-794-31)

Marketing

Marketing Status
Marketed Since 2024-06-10
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": "66ab68e0-e9f1-4576-8a95-6bbe3682fd9b", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["5c943206-6df8-4fc5-ab1d-d34b9715182c"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-794-30)", "package_ndc": "62332-794-30", "marketing_start_date": "20240610"}, {"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-794-31)", "package_ndc": "62332-794-31", "marketing_start_date": "20240610"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-794-71)", "package_ndc": "62332-794-71", "marketing_start_date": "20240610"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-794-90)", "package_ndc": "62332-794-90", "marketing_start_date": "20240610"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-794-91)", "package_ndc": "62332-794-91", "marketing_start_date": "20240610"}], "brand_name": "VENLAFAXINE HYDROCHLORIDE", "product_id": "62332-794_66ab68e0-e9f1-4576-8a95-6bbe3682fd9b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "62332-794", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE HYDROCHLORIDE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA217767", "marketing_category": "ANDA", "marketing_start_date": "20240610", "listing_expiration_date": "20261231"}