Package 71205-527-30

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 71205-527-30
Digits Only 7120552730
Product NDC 71205-527
Product ID 71205-527_64b95939-234b-41a2-aaad-c101884e223c
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-527-30)

Marketing

Marketing Status
Marketed Since 2021-01-27
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": "64b95939-234b-41a2-aaad-c101884e223c", "openfda": {"upc": ["0371205527303"], "unii": ["X2ELS050D8"], "rxcui": ["1738483"], "spl_set_id": ["ce168c41-a860-45f5-bae8-7b3d9b48d86a"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-527-30)", "package_ndc": "71205-527-30", "marketing_start_date": "20210127"}], "brand_name": "Paroxetine", "product_id": "71205-527_64b95939-234b-41a2-aaad-c101884e223c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71205-527", "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": "10 mg/1"}], "application_number": "ANDA203854", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20261231"}