Package 71205-198-90

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 71205-198-90
Digits Only 7120519890
Product NDC 71205-198
Description

90 TABLET, FILM COATED in 1 BOTTLE (71205-198-90)

Marketing

Marketing Status
Marketed Since 2019-01-01
Brand paroxetine
Generic paroxetine hydrochloride hemihydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "077517cd-4eee-4524-997c-fecc919b72c9", "openfda": {"upc": ["0371205198909"], "unii": ["X2ELS050D8"], "rxcui": ["1738511"], "spl_set_id": ["903e4ef1-487d-4b65-9038-b05ceaf74d19"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-198-30)", "package_ndc": "71205-198-30", "marketing_start_date": "20190101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-198-90)", "package_ndc": "71205-198-90", "marketing_start_date": "20190101"}], "brand_name": "Paroxetine", "product_id": "71205-198_077517cd-4eee-4524-997c-fecc919b72c9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71205-198", "generic_name": "paroxetine hydrochloride hemihydrate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA203854", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20261231"}