Package 69367-336-30

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 69367-336-30
Digits Only 6936733630
Product NDC 69367-336
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69367-336-30)

Marketing

Marketing Status
Marketed Since 2021-07-26
Brand paroxetine
Generic paroxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a272d00-5b37-47b2-870a-0028ca799109", "openfda": {"upc": ["0369367337304"], "unii": ["X2ELS050D8"], "rxcui": ["1738803", "1738805", "1738807"], "spl_set_id": ["f39a2a7a-7a7e-4dd8-9704-54d9598504fb"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69367-336-30)", "package_ndc": "69367-336-30", "marketing_start_date": "20210726"}], "brand_name": "Paroxetine", "product_id": "69367-336_0a272d00-5b37-47b2-870a-0028ca799109", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "69367-336", "generic_name": "Paroxetine", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA213485", "marketing_category": "ANDA", "marketing_start_date": "20210726", "listing_expiration_date": "20261231"}