Package 42806-601-10

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-601-10
Digits Only 4280660110
Product NDC 42806-601
Product ID 42806-601_4bde62db-14e4-fede-e063-6294a90a1391
Description

1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42806-601-10)

Marketing

Marketing Status
Marketed Since 2022-09-07
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": "4bde62db-14e4-fede-e063-6294a90a1391", "openfda": {"upc": ["0342806603093", "0342806601099", "0342806601303", "0342806602102", "0342806603307", "0342806603055", "0342806602096", "0342806602300", "0342806601105"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["430777f0-347c-4f21-8c5d-55f4e9897e74"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42806-601-09)", "package_ndc": "42806-601-09", "marketing_start_date": "20220907"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42806-601-10)", "package_ndc": "42806-601-10", "marketing_start_date": "20220907"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42806-601-30)", "package_ndc": "42806-601-30", "marketing_start_date": "20220907"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "42806-601_4bde62db-14e4-fede-e063-6294a90a1391", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "42806-601", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA214654", "marketing_category": "ANDA", "marketing_start_date": "20220907", "listing_expiration_date": "20271231"}