Package 55111-455-60

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55111-455-60
Digits Only 5511145560
Product NDC 55111-455
Description

60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-60)

Marketing

Marketing Status
Marketed Since 2011-06-01
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": "a0b75dbc-2382-70bc-7bd9-c6ef3ee4ed3e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["7027be98-61d6-a986-c9df-60ceef5f7ff0"], "manufacturer_name": ["Dr.Reddy's Laboratories Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-01)", "package_ndc": "55111-455-01", "marketing_start_date": "20110601"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-05)", "package_ndc": "55111-455-05", "marketing_start_date": "20110601"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-30)", "package_ndc": "55111-455-30", "marketing_start_date": "20110601"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-60)", "package_ndc": "55111-455-60", "marketing_start_date": "20110601"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-455-78)  / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (55111-455-79)", "package_ndc": "55111-455-78", "marketing_start_date": "20110601"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55111-455-90)", "package_ndc": "55111-455-90", "marketing_start_date": "20110601"}], "brand_name": "venlafaxine hydrochloride", "product_id": "55111-455_a0b75dbc-2382-70bc-7bd9-c6ef3ee4ed3e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "55111-455", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Dr.Reddy's Laboratories Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA078421", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}