Package 50090-6301-0

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6301-0
Digits Only 5009063010
Product NDC 50090-6301
Description

33 BLISTER PACK in 1 CARTON (50090-6301-0) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-12-29
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a374bf84-105a-4f9d-8303-2b27df2e7bff", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["8d6e699b-24bf-4e77-8a7f-acd496a700c7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "33 BLISTER PACK in 1 CARTON (50090-6301-0)  / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "50090-6301-0", "marketing_start_date": "20221229"}], "brand_name": "venlafaxine hydrochloride", "product_id": "50090-6301_a374bf84-105a-4f9d-8303-2b27df2e7bff", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-6301", "generic_name": "venlafaxine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA090174", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}