Package 70518-2532-4

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2532-4
Digits Only 7051825324
Product NDC 70518-2532
Description

30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2532-4)

Marketing

Marketing Status
Marketed Since 2023-12-07
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": "4a65d321-8f96-e5b9-e063-6294a90a6316", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["4e3053b9-cdec-4f4d-85ae-2e55cf1cc185"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2532-0)", "package_ndc": "70518-2532-0", "marketing_start_date": "20200108"}, {"sample": false, "description": "30 POUCH in 1 BOX (70518-2532-1)  / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-2532-2)", "package_ndc": "70518-2532-1", "marketing_start_date": "20230826"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2532-4)", "package_ndc": "70518-2532-4", "marketing_start_date": "20231207"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "70518-2532_4a65d321-8f96-e5b9-e063-6294a90a6316", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2532", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20200108", "listing_expiration_date": "20271231"}