Package 68071-2835-9

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 68071-2835-9
Digits Only 6807128359
Product NDC 68071-2835
Product ID 68071-2835_49dd0640-7879-15d0-e063-6294a90a7f47
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-2835-9)

Marketing

Marketing Status
Marketed Since 2026-02-02
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": "49dd0640-7879-15d0-e063-6294a90a7f47", "openfda": {"upc": ["0368071283594"], "unii": ["X2ELS050D8"], "rxcui": ["1738495"], "spl_set_id": ["49dd0858-685f-f46b-e063-6294a90a7f39"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-2835-9)", "package_ndc": "68071-2835-9", "marketing_start_date": "20260202"}], "brand_name": "Paroxetine", "product_id": "68071-2835_49dd0640-7879-15d0-e063-6294a90a7f47", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-2835", "generic_name": "paroxetine hydrochloride hemihydrate", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA203854", "marketing_category": "ANDA", "marketing_start_date": "20220329", "listing_expiration_date": "20271231"}