Package 68382-036-16

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68382-036-16
Digits Only 6838203616
Product NDC 68382-036
Product ID 68382-036_8c02c121-fe14-45f5-b2bc-b09fd377531f
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-16)

Marketing

Marketing Status
Marketed Since 2011-06-01
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": "8c02c121-fe14-45f5-b2bc-b09fd377531f", "openfda": {"upc": ["0368382034106", "0368382035103", "0368382036100"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["5351fe67-17d9-42ec-9e8b-6585fdb9e29e"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-06)", "package_ndc": "68382-036-06", "marketing_start_date": "20110601"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-10)", "package_ndc": "68382-036-10", "marketing_start_date": "20110601"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-16)", "package_ndc": "68382-036-16", "marketing_start_date": "20110601"}], "brand_name": "venlafaxine hydrochloride", "product_id": "68382-036_8c02c121-fe14-45f5-b2bc-b09fd377531f", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68382-036", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA 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"}