Package 68180-645-06

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 68180-645-06
Digits Only 6818064506
Product NDC 68180-645
Product ID 68180-645_1a9bc25c-db83-42a0-851a-30212ee10cc6
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-645-06)

Marketing

Marketing Status
Marketed Since 2017-03-06
Brand paroxetine
Generic paroxetine
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": "1a9bc25c-db83-42a0-851a-30212ee10cc6", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738803", "1738805", "1738807"], "spl_set_id": ["d315e0da-f829-408b-be5d-2bca2e06913c"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-645-06)", "package_ndc": "68180-645-06", "marketing_start_date": "20170306"}], "brand_name": "PAROXETINE", "product_id": "68180-645_1a9bc25c-db83-42a0-851a-30212ee10cc6", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68180-645", "generic_name": "PAROXETINE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAROXETINE", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "37.5 mg/1"}], "application_number": "ANDA204134", "marketing_category": "ANDA", "marketing_start_date": "20170306", "listing_expiration_date": "20261231"}