Package 42708-054-30

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-054-30
Digits Only 4270805430
Product NDC 42708-054
Product ID 42708-054_45b3e0e2-7ec5-7419-e063-6394a90a2f2a
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42708-054-30)

Marketing

Marketing Status
Marketed Since 2018-03-14
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package Yes

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45b3e0e2-7ec5-7419-e063-6394a90a2f2a", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["9e745ad7-be4f-4369-be23-587e1154e4ab"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42708-054-30)", "package_ndc": "42708-054-30", "marketing_start_date": "20180314"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "42708-054_45b3e0e2-7ec5-7419-e063-6394a90a2f2a", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "42708-054", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA076565", "marketing_category": "ANDA", "marketing_start_date": "20100701", "listing_expiration_date": "20261231"}