Package 62135-531-30

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-531-30
Digits Only 6213553130
Product NDC 62135-531
Description

30 TABLET in 1 BOTTLE (62135-531-30)

Marketing

Marketing Status
Marketed Since 2023-03-29
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": "45adb66f-add1-678a-e063-6394a90a1f26", "openfda": {"upc": ["0362135531300"], "unii": ["7D7RX5A8MO"], "rxcui": ["808748"], "spl_set_id": ["85ec2d3f-49e4-4ac5-bd4a-c227589dbf58"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62135-531-30)", "package_ndc": "62135-531-30", "marketing_start_date": "20230329"}], "brand_name": "venlafaxine hydrochloride", "product_id": "62135-531_45adb66f-add1-678a-e063-6394a90a1f26", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "62135-531", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA209193", "marketing_category": "ANDA", "marketing_start_date": "20191226", "listing_expiration_date": "20261231"}