Package 55154-7999-0

Brand: paroxetine

Generic: paroxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-7999-0
Digits Only 5515479990
Product NDC 55154-7999
Product ID 55154-7999_224dfb62-6c9f-435c-b760-434430075a5c
Description

1 BLISTER PACK in 1 BAG (55154-7999-0) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2003-09-08
Brand paroxetine
Generic paroxetine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "224dfb62-6c9f-435c-b760-434430075a5c", "openfda": {"unii": ["3I3T11UD2S"], "rxcui": ["1738495"], "spl_set_id": ["333dfd07-61f0-4b86-b4b5-b04adf64e49f"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 BAG (55154-7999-0)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-7999-0", "marketing_start_date": "20030908"}], "brand_name": "PAROXETINE", "product_id": "55154-7999_224dfb62-6c9f-435c-b760-434430075a5c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55154-7999", "generic_name": "paroxetine hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAROXETINE", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE ANHYDROUS", "strength": "20 mg/1"}], "application_number": "ANDA075356", "marketing_category": "ANDA", "marketing_start_date": "20030908", "listing_expiration_date": "20261231"}