Package 70518-2871-0

Brand: paroxetine

Generic: paroxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2871-0
Digits Only 7051828710
Product NDC 70518-2871
Product ID 70518-2871_4b051cf4-2456-e66e-e063-6294a90af78e
Description

100 POUCH in 1 BOX (70518-2871-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-2871-1)

Marketing

Marketing Status
Marketed Since 2020-09-08
Brand paroxetine
Generic paroxetine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b051cf4-2456-e66e-e063-6294a90af78e", "openfda": {"unii": ["3I3T11UD2S"], "rxcui": ["1738495"], "spl_set_id": ["98d4f767-06e3-4d9b-b1ad-4b31f7e36130"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2871-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-2871-1)", "package_ndc": "70518-2871-0", "marketing_start_date": "20200908"}], "brand_name": "PAROXETINE", "product_id": "70518-2871_4b051cf4-2456-e66e-e063-6294a90af78e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-2871", "generic_name": "paroxetine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAROXETINE", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE ANHYDROUS", "strength": "20 mg/1"}], "application_number": "ANDA075356", "marketing_category": "ANDA", "marketing_start_date": "20200908", "listing_expiration_date": "20271231"}