Package 62175-472-41

Brand: paroxetine hydrochloride

Generic: paroxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62175-472-41
Digits Only 6217547241
Product NDC 62175-472
Product ID 62175-472_9474f942-d6d8-486b-8ea6-f8c561bb5014
Description

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-472-41)

Marketing

Marketing Status
Marketed Since 2014-10-31
Brand paroxetine hydrochloride
Generic paroxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Paroxetine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9474f942-d6d8-486b-8ea6-f8c561bb5014", "openfda": {"upc": ["0362175470324"], "unii": ["X2ELS050D8"], "rxcui": ["1738803", "1738805", "1738807"], "spl_set_id": ["f22886f5-230c-47e4-9dd8-ffb14c8d6ae4"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-472-32)", "package_ndc": "62175-472-32", "marketing_start_date": "20141031"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-472-41)", "package_ndc": "62175-472-41", "marketing_start_date": "20141031"}], "brand_name": "Paroxetine Hydrochloride", "product_id": "62175-472_9474f942-d6d8-486b-8ea6-f8c561bb5014", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "62175-472", "generic_name": "Paroxetine Hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine Hydrochloride", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA204744", "marketing_category": "ANDA", "marketing_start_date": "20141031", "listing_expiration_date": "20261231"}