Package 70518-1253-1

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 70518-1253-1
Digits Only 7051812531
Product NDC 70518-1253
Product ID 70518-1253_48c31a65-991c-7da8-e063-6294a90aac40
Description

30 POUCH in 1 BOX (70518-1253-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1253-2)

Marketing

Marketing Status
Marketed Since 2022-01-14
Brand paroxetine
Generic paroxetine hydrochloride hemihydrate
Sample Package No

Linked Drug Pages (1)

Paroxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48c31a65-991c-7da8-e063-6294a90aac40", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738511"], "spl_set_id": ["22174520-4b78-4841-96f7-530ba12d2cf1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-1253-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-1253-2)", "package_ndc": "70518-1253-1", "marketing_start_date": "20220114"}], "brand_name": "Paroxetine", "product_id": "70518-1253_48c31a65-991c-7da8-e063-6294a90aac40", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-1253", "generic_name": "paroxetine hydrochloride hemihydrate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA203854", "marketing_category": "ANDA", "marketing_start_date": "20180612", "listing_expiration_date": "20271231"}