Package 71209-028-05

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 71209-028-05
Digits Only 7120902805
Product NDC 71209-028
Description

100 TABLET in 1 BOTTLE (71209-028-05)

Marketing

Marketing Status
Marketed Since 2018-12-03
Brand venlafaxine
Generic venlafaxine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f6bcbdd6-db09-4aeb-8eb0-6eadb8ebdeba", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["2ed61dcf-42e3-47cf-a607-459eef5fea98"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71209-028-05)", "package_ndc": "71209-028-05", "marketing_start_date": "20181203"}], "brand_name": "VENLAFAXINE", "product_id": "71209-028_f6bcbdd6-db09-4aeb-8eb0-6eadb8ebdeba", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71209-028", "generic_name": "venlafaxine", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA206250", "marketing_category": "ANDA", "marketing_start_date": "20181203", "listing_expiration_date": "20261231"}