Package 72189-147-28

Brand: desvenlafaxine

Generic: desvenlafaxine succinate
NDC Package

Package Facts

Identity

Package NDC 72189-147-28
Digits Only 7218914728
Product NDC 72189-147
Description

28 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-147-28)

Marketing

Marketing Status
Marketed Since 2020-11-12
Brand desvenlafaxine
Generic desvenlafaxine succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be9051e-2257-8882-e063-6294a90a543a", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1874559"], "spl_set_id": ["b3ef2bb2-c336-2d57-e053-2995a90a5fe0"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-147-28)", "package_ndc": "72189-147-28", "marketing_start_date": "20201112"}], "brand_name": "desvenlafaxine", "product_id": "72189-147_2be9051e-2257-8882-e063-6294a90a543a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72189-147", "generic_name": "desvenlafaxine succinate", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204003", "marketing_category": "ANDA", "marketing_start_date": "20201112", "listing_expiration_date": "20261231"}