Package 68071-4442-9

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4442-9
Digits Only 6807144429
Product NDC 68071-4442
Product ID 68071-4442_1a8c4239-97e0-39ec-e063-6394a90a045b
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-4442-9)

Marketing

Marketing Status
Marketed Since 2018-05-21
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (1)

venlafaxine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1a8c4239-97e0-39ec-e063-6394a90a045b", "openfda": {"upc": ["0368071444292"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["6cb943a8-5972-292f-e053-2991aa0ae3ee"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-4442-9)", "package_ndc": "68071-4442-9", "marketing_start_date": "20180521"}], "brand_name": "venlafaxine hydrochloride", "product_id": "68071-4442_1a8c4239-97e0-39ec-e063-6394a90a045b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-4442", "generic_name": "venlafaxine hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20110601", "listing_expiration_date": "20261231"}